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US4331560A Expired / Lapsed US ⏱️ 0.0 years remaining

Catalyst and process for preparing organic isocyanates

Assignee: Chevron USA Inc
•
Filing: 1981-04-20
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Granted: 1982-05-25
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Expires: 2001-04-20
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Abstract

Abstract Organic isocyanates are prepared by reacting an organic nitrocompound with carbon monoxide in the presence of a novel catalyst system. The catalyst system is comprised of a noble metal compound, a heteroaromatic nitrogen compound, and an oxide of thorium or uranium.

Inventors

  • 👤 Wayne R. Pretzer
  • 👤 Richard B. Pannell

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 18:49
CPC Classifications
B; B01; B01J; B01J31/00; B01J31/16; B01J31/18; B01J31/1805; B01J31/181; B01J31/1825; B01J31/26; B01J31/28; B01J31/30; C; C07; C07C; C07C263/00; C07C263/14; B01J23/00; B01J23/12; B01J2531/00; B01J2531/80; B01J2531/82; B01J2531/822; B01J2531/824; B01J31/02; B01J31/0234; B01J31/0235; B01J31/0244

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 135 words
A process for preparing an organic isocyanate, which comprises: reacting an organic nitro compound with carbon monoxide in the presence of a catalyst comprised of (a) a noble metal compound, (b) a heteroaromatic nitrogen compound having a ring with (1) between five and six members in the ring, (2) only nitrogen and carbon in the ring, (3) no more than two nitrogens in the ring, and (4) containing at least two double bonds in the ring, wherein the molar ratio of the heteroaromatic nitrogen compound to the nobel metal compound lies between about 0.1 to 1 and 20 to 1, (c) an actinide oxide selected from the oxides of uranium and thorium, wherein the weight ratio of the noble metal compound to the actinide oxide lies between about 0.001 to 1 and 50 to 1.
Claim 2
Dependent Claim 135 words
A process for preparing an organic isocyanate, which comprises: reacting an organic nitro compound with carbon monoxide in the presence of a catalyst comprised of (a) a noble metal compound, (b) a heteroaromatic nitrogen compound having a ring with (1) between five and six members in the ring, (2) only nitrogen and carbon in the ring, (3) no more than two nitrogens in the ring, and (4) containing at least two double bonds in the ring, wherein the molar ratio of the heteroaromatic nitrogen compound to the nobel metal compound lies between about 0.1 to 1 and 20 to 1, (c) an actinide oxide selected from the oxides of uranium and thorium, wherein the weight ratio of the noble metal compound to the actinide oxide lies between about 0.001 to 1 and 50 to 1.
Claim 3
Dependent Claim 36 words
The process of claim 1, wherein said noble metal compound is selected from the group consisting of noble metals, noble metal halides, noble metal oxides, organic salts of noble metals and organic complexes of noble metals.
Claim 4
Dependent Claim 58 words
The process of claim 2, wherein the heteroaromatic nitrogen compound is selected from the group consisting of (a) pyridine (b) 2,6-dimethyl pyridine (c) 2,4,6-trimethyl pyridine (d) 4-phenyl pyridine (e) 3-chloro pyridine (f) lauryl pyridium chloride (g) quinoline (h) 7,8 benzo quinoline (i) 2-chloro quinoline (j) isoquinoline (k) benzo isoquinoline (l) imidazole (m) picolinic acid (n) 4-picoline-1-oxide (o) 3-picoline-1-oxide
Claim 5
Dependent Claim 134 words
A process for preparing an aromatic isocyanate, which comprises: reacting an aromatic nitro compound with carbon monoxide in the presence of a catalyst comprised of (a) a noble metal compound, (b) a heteroaromatic nitrogen compound having a ring with (1) between five and six members in the ring, (2) only nitrogen and carbon in the ring, (3) no more than two nitrogens in the ring, and (4) at least two double bonds in the ring, wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.1 to 1 and 20 to 1, (c) an actinide oxide selected from the oxides of uranium or thorium, wherein the weight ratio of the noble metal compound to the actinide oxide lies between about 0.001 to 1 and 50 to 1.
Claim 6
Dependent Claim 134 words
A process for preparing an aromatic isocyanate, which comprises: reacting an aromatic nitro compound with carbon monoxide in the presence of a catalyst comprised of (a) a noble metal compound, (b) a heteroaromatic nitrogen compound having a ring with (1) between five and six members in the ring, (2) only nitrogen and carbon in the ring, (3) no more than two nitrogens in the ring, and (4) at least two double bonds in the ring, wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.1 to 1 and 20 to 1, (c) an actinide oxide selected from the oxides of uranium or thorium, wherein the weight ratio of the noble metal compound to the actinide oxide lies between about 0.001 to 1 and 50 to 1.
Claim 7
Dependent Claim 37 words
The process of claim 4, wherein the said noble metal compound is selected from the group consisting of noble metals, noble metal halides, noble metal oxides, organic salts of noble metals and organic complexes of noble metals.
Claim 8
Dependent Claim 58 words
The process of claim 5, wherein the said heteroaromatic compound is selected from the group consisting of (a) pyridine (b) 2,6-dimethyl pyridine (c) 2,4,6-trimethyl pyridine (d) 4-phenyl pyridine (e) 3-chloro pyridine (f) lauryl pyridium chloride (g) quinoline (h) 7,8 benzo quinoline (i) 2-chloro quinoline (j) isoquinoline (k) benzo isoquinoline (l) imidazole (m) picolinic acid (n) 4-picoline-1-oxide (o) 3-picoline-1-oxide
Claim 9
Dependent Claim 124 words
A process for preparing an aromatic, isocyanate which comprises: reacting an aromatic nitro compound with carbon monoxide in the presence of (a) a noble metal chloride selected from the group consisting of the chlorides of palladium and rhodium, (b) a heteroaromatic nitrogen compound selected from the group consisting of pyridine, quinoline, and isoquinoline, (c) an actinide oxide selected from the group consisting of U 2 O 5 , U 3 O 8 , and ThO 2 , wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.5 to 1 and 10 to 1 and the weight ratio of the noble metal compound to the actinide oxide lies between about 0.05 to 1 and 25 to 1.
Claim 10
Dependent Claim 124 words
A process for preparing an aromatic, isocyanate which comprises: reacting an aromatic nitro compound with carbon monoxide in the presence of (a) a noble metal chloride selected from the group consisting of the chlorides of palladium and rhodium, (b) a heteroaromatic nitrogen compound selected from the group consisting of pyridine, quinoline, and isoquinoline, (c) an actinide oxide selected from the group consisting of U 2 O 5 , U 3 O 8 , and ThO 2 , wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.5 to 1 and 10 to 1 and the weight ratio of the noble metal compound to the actinide oxide lies between about 0.05 to 1 and 25 to 1.
Claim 11
Dependent Claim 139 words
A catalyst system useful in the preparation of organic isocyanates from the corresponding organic nitro compounds, which comprises in combination: (a) a noble metal compound, (b) a heteroaromatic nitrogen compound having a ring with, (1) between five and six members in the ring, (2) only nitrogen and carbon in the ring, (3) no more than two nitrogens in the ring, (4) at least two double bonds in the ring, wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.1 to 1 and 20 to 1, (c) an actinide oxide selected from the group consisting of U 2 O 5 , U 3 O 8 and ThO 2 , wherein the weight ratio of the noble metal compound to the actinide oxide lies between about 0.001 to 1 and 50 to 1.
Claim 12
Dependent Claim 139 words
A catalyst system useful in the preparation of organic isocyanates from the corresponding organic nitro compounds, which comprises in combination: (a) a noble metal compound, (b) a heteroaromatic nitrogen compound having a ring with, (1) between five and six members in the ring, (2) only nitrogen and carbon in the ring, (3) no more than two nitrogens in the ring, (4) at least two double bonds in the ring, wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.1 to 1 and 20 to 1, (c) an actinide oxide selected from the group consisting of U 2 O 5 , U 3 O 8 and ThO 2 , wherein the weight ratio of the noble metal compound to the actinide oxide lies between about 0.001 to 1 and 50 to 1.
Claim 13
Dependent Claim 39 words
A catalyst system as in claim 8 wherein, the said noble metal compound is selected from the group consisting of noble metals, noble metal halides, noble metal oxides, organic salts of noble metals and organic complexes of noble metals.
Claim 14
Dependent Claim 61 words
A catalyst system as in claim 9 wherein, the said heteroaromatic nitrogen compound is selected from the group consisting of (a) pyridine (b) 2,6-dimethyl pyridine (c) 2,4,6-trimethyl pyridine (d) 4-phenyl pyridine (e) 3-chloro pyridine (f) lauryl pyridium chloride (g) quinoline (h) 7,8 benzo quinoline (i) 2-chloro quinoline (j) isoquinoline (k) benzo isoquinoline (l) imidazole (m) picolinic acid (n) 4-picoline-1-oxide (o) 3-picoline-1-oxide
Claim 15
Dependent Claim 123 words
A catalyst system useful in the preparation of aromatic isocyanates from the corresponding aromatic nitro compound, which comprises in combination: (a) a noble metal chloride selected from the group consisting of the chlorides of palladium and rhodium, (b) a heteroaromatic nitrogen compound selected from the group consisting of pyridine, quinoline, and isoquinoline, (c) an actinide oxide selected from the group consisting of U 2 O 5 , U 3 O 8 , and ThO 2 , wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.5 to 1 and 10 to 1 and the weight ratio of the noble metal compound to the actinide oxide lies between about 0.05 to 1 and 25 to 1.
Claim 16
Dependent Claim 123 words
A catalyst system useful in the preparation of aromatic isocyanates from the corresponding aromatic nitro compound, which comprises in combination: (a) a noble metal chloride selected from the group consisting of the chlorides of palladium and rhodium, (b) a heteroaromatic nitrogen compound selected from the group consisting of pyridine, quinoline, and isoquinoline, (c) an actinide oxide selected from the group consisting of U 2 O 5 , U 3 O 8 , and ThO 2 , wherein the molar ratio of the heteroaromatic nitrogen compound to the noble metal compound lies between about 0.5 to 1 and 10 to 1 and the weight ratio of the noble metal compound to the actinide oxide lies between about 0.05 to 1 and 25 to 1.

References Cited (Backward Citations)

US3576835A Cited
US3674827A Cited
US4267070A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-05-24 1985-11-23 1986-05-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-05-24 1989-11-23 1990-05-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-05-24 1993-11-23 1994-05-25 $7700.00 Window Closed / Lapsed

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