US4080365A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Process for preparing aromatic urethanes
Assignee: Mitsui Toatsu Chemicals Inc
•
Filing: 1976-05-19
•
Granted: 1978-03-21
•
Expires: 1996-05-19
Abstract
Abstract Aromatic urethanes can be produced in exceedingly improved yield when an aromatic nitro compound, an organic compound containing hydroxyl groups, and carbon monoxide are reacted in the presence of a catalyst composed of metallic (elemental) selenium or a selenium compound and a base serving as promoter, to which reaction system an aromatic amino compound and/or an aromatic urea compound which will be secondarily produced by the reaction has been previously added in order to suppress side reactions. For instance, when nitrobenzene, methanol and carbon monoxide are interacted in the presence of metallic selenium and triethylenediamine, the conversion of nitrobenzene is 68% and the percentage of formed methyl N-phenylcarbamate to the interacted nitrobenzene is 80%, whereas when the reaction is effected under the same reaction conditions indicated above with addition to the reaction system of aniline in an amount of about 15 wt. % of the nitrobenzene, the conversion of nitrobenzene and the percentage of formed methyl N-phenylcarbamate reach 100% and 98%, respectively.
Inventors
- 👤 Yutaka Hirai
- 👤 Katsuharu Miyata
- 👤 Seiji Hasegawa
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 21:10
CPC Classifications
C; C07; C07C; C07C271/00; C07C271/06
Claims Analysis
Total Claims: 10
Claim 1
Independent Claim
386 words
In a process for preparing an aromatic urethane which comprises interacting an aromatic nitro compound expressed by formula (1) A--(NO.sub.2).sub.x ( 1) wherein A represents the residue of an aromatic nitro compound from which nitro groups are removed, and x is an integer of from 1 to 4, an alcohol expressed by formula (2) R--OH (2) wherein R represents a linear or branched alkyl group containing from 1 to 16 carbon atoms, a cycloalkyl group having 6 carbon atoms with or without an alkyl substituent containing from 1 to 3 carbon atoms, or an aralkyl group having an alkyl moiety containing from 1 to 6 carbon atoms, and carbon monoxide in the presence of a selenium-containing catalytic system, the improvement which comprises adding to the reaction system at least one compound selected from the group consisting of an aromatic amino compound expressed by formula (3) ##STR5## wherein A and x have the same meanings as defined in formula (1), respectively, y is an integer of from 1 to 4, z is an integer of from 0 to 3, the total number of y and z not exceeding x, and R has the same meaning as defined in formula (2) and aromatic urea compounds expressed by formula (4) ##STR6## wherein A and x, R, and y and z have, respectively, the same meanings as defined in formulae (1), (2) and (3), y' is an integer of from 1 to 4, z' is an integer of from 0 to 3, the total number of y' and z' not exceeding x, and a, b and c are each 0 when x = 1 or 2, one of a, b or c is 1 and the other two is 0 when x = 3, one of a, b or c is 2 and the other two are 0 or any two of a, b and c are 1 and the other is 0 when x = 4, and n is 0 when x = 1 and n is an integer of from 0 to 3 when x = 2 - 4, whereby there is obtained at high yield an aromatic urethane expressed by formula (5) A--(NHCO.sub.2 R).sub.x ( 5) wherein A and x have the same meanings as defined in formula (1), respectively, and R as defined in formula (2).
Claim 2
Dependent Claim
386 words
In a process for preparing an aromatic urethane which comprises interacting an aromatic nitro compound expressed by formula (1) A--(NO.sub.2).sub.x ( 1) wherein A represents the residue of an aromatic nitro compound from which nitro groups are removed, and x is an integer of from 1 to 4, an alcohol expressed by formula (2) R--OH (2) wherein R represents a linear or branched alkyl group containing from 1 to 16 carbon atoms, a cycloalkyl group having 6 carbon atoms with or without an alkyl substituent containing from 1 to 3 carbon atoms, or an aralkyl group having an alkyl moiety containing from 1 to 6 carbon atoms, and carbon monoxide in the presence of a selenium-containing catalytic system, the improvement which comprises adding to the reaction system at least one compound selected from the group consisting of an aromatic amino compound expressed by formula (3) ##STR5## wherein A and x have the same meanings as defined in formula (1), respectively, y is an integer of from 1 to 4, z is an integer of from 0 to 3, the total number of y and z not exceeding x, and R has the same meaning as defined in formula (2) and aromatic urea compounds expressed by formula (4) ##STR6## wherein A and x, R, and y and z have, respectively, the same meanings as defined in formulae (1), (2) and (3), y' is an integer of from 1 to 4, z' is an integer of from 0 to 3, the total number of y' and z' not exceeding x, and a, b and c are each 0 when x = 1 or 2, one of a, b or c is 1 and the other two is 0 when x = 3, one of a, b or c is 2 and the other two are 0 or any two of a, b and c are 1 and the other is 0 when x = 4, and n is 0 when x = 1 and n is an integer of from 0 to 3 when x = 2 - 4, whereby there is obtained at high yield an aromatic urethane expressed by formula (5) A--(NHCO.sub.2 R).sub.x ( 5) wherein A and x have the same meanings as defined in formula (1), respectively, and R as defined in formula (2).
Claim 3
Dependent Claim
17 words
The process according to claim 1 wherein said aromatic nitro compound expressed by formula (1) is dinitrotoluene.
Claim 4
Dependent Claim
16 words
The process according to claim 1, wherein said alcohol expressed by formula (2) is ethyl alcohol.
Claim 5
Dependent Claim
50 words
The process according to claim 1, wherein said aromatic nitro compound expressed by formula (1) is 2,4-dinitrotoluene, said alcohol expressed by formula (2) is ethyl alcohol, and said aromatic amino compound expressed by formula (3) is a member selected from the group consisting of 2-amino-4-ethylcarbamatetoluene, 4-amino-2-ethylcarbamatetoluene, 2-amino-4-nitrotoluene, 4-amino-2-nitrotoluene and 2,4-diaminotoluene.
Claim 6
Dependent Claim
48 words
The process according to claim 1, wherein said aromatic nitro compound expressed by formula (1) is 2,6-dinitrotoluene, said alcohol expressed by formula (2) is ethyl alcohol, and said aromatic amino compound expressed by formula (3) is a compound selected from the group consisting of 2-amino-6-nitrotoluene, 2-amino-6-ethylcarbamatetoluene and 2,6-diaminotoluene.
Claim 7
Dependent Claim
69 words
The process according to claim 1, wherein said aromatic nitro compound expressed by formula (1) is 2,4-dinitrotoluene, said alcohol expressed by formula (2) is ethyl alcohol, and said aromatic urea compound expressed by formula (4) is at least one compound selected from the group consisting of 1,3-bis(3-nitro-4-methylphenyl)urea, 1,3-bis-(2-methyl-5-nitrophenyl)urea, 1,3-bis(3-ethylcarbamate-4-methylphenyl)urea, 1,3-bis(2-methyl-5-ethylcarbamatephenyl)urea, 1,3-bis(3-amino-4-methylphenyl)urea, 1,3-bis(2-methyl-5-aminophenyl)urea, 1-(3-nitro-4-methylphenyl)-3-(2-methyl-5-nitrophenyl)urea, 1-(3-ethylcarbamate-4-methylphenyl)-3-(2-methyl-5-ethylcarbamatephenyl)urea, 1-(3-amino-4-methylphenyl)-3-(2-methyl-5-aminophenyl)urea, 1-(3-nitro-4-methylphenyl)-3-(3-ethylcarbamate-4-methylphenyl)urea, 1-(3-nitro-4-methylphenyl)-3-(2-methyl-5-ethylcarbamatephenyl)urea, 1-(3-nitro-4-methylphenyl)-3-(3-amino-4-methylphenyl)urea, 1-(3-nitro-4-methylphenyl)-3-(2-methyl-5-aminophenyl)urea, 1-(2-methyl-5-nitrophenyl)-3-(3-ethylcarbamate-4-methylphenyl)urea, 1-(2-methyl-5-nitrophenyl)-3-(2-methyl-5-ethylcarbamatephenyl)urea, 1-(2-methyl-5-nitrophenyl)-3-(3-amino-4-methylphenyl)urea, 1-(2-methyl-5-nitrophenyl)-3-(2-methyl-5-aminophenyl)urea, 1-(3-ethylcarbamate-4-methylphenyl)-3-(3-amino-4-methylphenyl)urea, 1-(3-ethylcarbamate-4-methylphenyl-3-(2-methyl-5-aminophenyl urea, 1-(2-methyl-5-ethylcarbamatephenyl)-3-(3-amino-4-methylphenyl)urea and 1-(2-methyl-5-ethylcarbamatephenyl)-3-(2-methyl-5-aminophenyl)urea.
Claim 8
Dependent Claim
54 words
The process according to claim 1, wherein said aromatic nitro compound expressed by formula (1) is 2,6-dinitrotoluene, said alcohol expressed by formula (2) is ethyl alcohol, and said aromatic urea compound expressed by formula (4) is at least one compound selected from the group consisting of 1,3-bis(2-methyl-3-nitrophenyl)urea, 1,3-bis(2-methyl-3-ethylcarbamatephenyl)urea, 1,3-bis(2-methyl-3-aminophenyl)urea, 1-(2-methyl-3-nitrophenyl-3-(2-methyl-3-ethylcarbamatephenyl)urea, 1-(2-methyl-3-nitrophenyl)-3-(2-methyl-3-aminophenyl)urea, and 1-(2-methyl-3-ethylcarbamatephenyl)-3-(2-methyl-3-aminophenyl urea.
Claim 9
Dependent Claim
44 words
The process according to claim 1, wherein said selenium-containing catalytic system is composed of (a) a catalyst selected from the group consisting of elemental selenium and selenium dioxide and (b) a promoter selected from the group consisting of potassium acetate, sodium acetate and triethylenediamine.
Claim 10
Dependent Claim
39 words
The process according to claim 1, wherein said selenium-containing catalytic system is composed of (a) a catalyst selected from the group consisting of elemental selenium and selenium dioxide and (b) a promoter consisting of 1,8-diazabicyclo (5,4,0)-undecene-7 and acetic acid.
References Cited (Backward Citations)
US3956360A
Cited
US3993685A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1981-03-20 | 1981-09-19 | 1982-03-21 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1985-03-20 | 1985-09-19 | 1986-03-21 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1989-03-20 | 1989-09-19 | 1990-03-21 | $7700.00 | Window Closed / Lapsed |