US3953480A
Expired / Lapsed
US
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Epoxidation of olefins by hydrogen peroxide
Assignee: Produits Chimiques Ugine Kuhlmann
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Filing: 1974-09-30
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Granted: 1976-04-27
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Expires: 1994-09-30
Abstract
Abstract An oxirane compound is prepared by reacting an olefinically unsaturated compound with hydrogen peroxide in the presence both of (i) at least one lead compound, exemplarily triethyl lead hydroxide and also of (ii) at least one compound of a group IV-A, V-A or VI-A transition metal exemplarily tungsten hexacarbonyl. The epoxided products are useful in the manufacture of plastics, adhesives and the like.
Inventors
- 👤 Serge Delavarenne
- 👤 Francis Weiss
- 👤 Jean-Pierre Schirmann
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-04 22:07
CPC Classifications
B; B01; B01J; B01J31/00; B01J31/02; B01J31/12; B01J31/122; B01J31/16; B01J31/20; C; C07; C07D; C07D301/00; C07D301/02; C07D301/03; C07D301/12; C07D303/00; C07D303/02; C07D303/04; B01J2231/00; B01J2231/70; B01J2231/72; B01J2531/00; B01J2531/40; B01J2531/44; B01J2531/60; B01J2531/64; B01J2531/66; Y; Y02; Y02P; Y02P20/00; Y02P20/50; Y02P20/52
Claims Analysis
Total Claims: 12
Claim 1
Independent Claim
212 words
A method for preparing an oxirane compound which comprises reacting an olefin with hydrogen peroxide in a solvent selected from a lower alkanol, a nitrile, an amide, and an ether, in the presence of a catalyst system including: a. molybdenum hexacarbonyl or tungsten hexacarbonyl, or a mixture thereof; and b. an organolead compound of tetravalent lead having from one to three of its four valences bonded to an organic group which is a straight-chained C 1 -C 12 alkyl radical, a C 3 -C 12 branched or cyclic alkyl radical, a C 3 -C 11 straight-chained alkylene radical, or a C 6 -C 12 aryl radical, and having the remainder of its four valences bonded to at least one anionic group which is a hydroxyl group or a group which is convertible to a hydroxyl or hydroperoxyl group in the presence of aqueous hydrogen peroxide, said convertible group being a halogen or an anion of a mineral or organic acid, or a C 1 -C 12 alkoxy or phenoxy group or an oxide anion formed by the loss of a proton from an organolead hydroxide, wherein said organic groups can be identical to or different from each other and wherein said anionic groups can be identical to or different from each other.
Claim 2
Independent Claim
212 words
A method for preparing an oxirane compound which comprises reacting an olefin with hydrogen peroxide in a solvent selected from a lower alkanol, a nitrile, an amide, and an ether, in the presence of a catalyst system including: a. molybdenum hexacarbonyl or tungsten hexacarbonyl, or a mixture thereof; and b. an organolead compound of tetravalent lead having from one to three of its four valences bonded to an organic group which is a straight-chained C 1 -C 12 alkyl radical, a C 3 -C 12 branched or cyclic alkyl radical, a C 3 -C 11 straight-chained alkylene radical, or a C 6 -C 12 aryl radical, and having the remainder of its four valences bonded to at least one anionic group which is a hydroxyl group or a group which is convertible to a hydroxyl or hydroperoxyl group in the presence of aqueous hydrogen peroxide, said convertible group being a halogen or an anion of a mineral or organic acid, or a C 1 -C 12 alkoxy or phenoxy group or an oxide anion formed by the loss of a proton from an organolead hydroxide, wherein said organic groups can be identical to or different from each other and wherein said anionic groups can be identical to or different from each other.
Claim 3
Dependent Claim
14 words
The method of claim 1 wherein the organolead compound is triethyl lead dihydrogen phosphate.
Claim 4
Dependent Claim
20 words
The method of claim 1 wherein the catalyst system is a mixture of triethyl lead dihydrogen phosphate and tungsten hexacarbonyl.
Claim 5
Dependent Claim
58 words
The method of claim 1 wherein the reaction takes place at between about 0° and 100°C and at between about 1 and 100 atmospheres and wherein each of a. molybdenum hexacarbonyl or the tungsten hexacarbonyl, or the mixture thereof, and b. the organolead compound comprises about 0.01 to 10% based on the weight of the total reaction mixture.
Claim 6
Dependent Claim
41 words
The method of claim 1 wherein at least one of the organic groups bonded to the lead is substituted by a halogen atom or a hydroxy, nitro, nitroso, methoxy, C 1 -C 12 alkoxy, amino, carboxyl, ester, amide, or nitrile group.
Claim 7
Independent Claim
209 words
A method for epoxidizing cyclohexene which comprises reacting cyclohexene with hydrogen peroxide in a solvent selected from a lower alkanol, a nitrile, an amide, and an ether, in the presence of a catalyst system including: a. molybdenum hexacarbonyl or tungsten hexacarbonyl, or a mixture thereof; and b. an organolead compound of tetravalent lead having from one to three of its four valences bonded to an organic group which is a straight-chained C 1 -C 12 alkyl radical, a C 3 -C 12 branched or cyclic alkyl radical, a C 3 -C 11 straight-chained alkylene radical, or a C 6 -C 12 aryl radical, and having the remainder of its four valences bonded to at lest one anionic group which is a hydroxyl group or a group which is convertible to a hydroxyl or hydroperoxyl group in the presence of aqueous hydrogen peroxide, said convertible group being a halogen or an anion of a mineral or organic acid, or a C 1 -C 12 alkoxy or phenoxy group or an oxide anion formed by the loss of a proton from an organolead hydroxide, wherein said organic groups can be identical to or different from each other and wherein said anionic groups can be identical to or different from each other.
Claim 8
Independent Claim
209 words
A method for epoxidizing cyclohexene which comprises reacting cyclohexene with hydrogen peroxide in a solvent selected from a lower alkanol, a nitrile, an amide, and an ether, in the presence of a catalyst system including: a. molybdenum hexacarbonyl or tungsten hexacarbonyl, or a mixture thereof; and b. an organolead compound of tetravalent lead having from one to three of its four valences bonded to an organic group which is a straight-chained C 1 -C 12 alkyl radical, a C 3 -C 12 branched or cyclic alkyl radical, a C 3 -C 11 straight-chained alkylene radical, or a C 6 -C 12 aryl radical, and having the remainder of its four valences bonded to at lest one anionic group which is a hydroxyl group or a group which is convertible to a hydroxyl or hydroperoxyl group in the presence of aqueous hydrogen peroxide, said convertible group being a halogen or an anion of a mineral or organic acid, or a C 1 -C 12 alkoxy or phenoxy group or an oxide anion formed by the loss of a proton from an organolead hydroxide, wherein said organic groups can be identical to or different from each other and wherein said anionic groups can be identical to or different from each other.
Claim 9
Dependent Claim
14 words
The method of claim 6 wherein the organolead compound is triethyl lead dihydrogen phosphate.
Claim 10
Dependent Claim
20 words
The method of claim 6 wherein the catalyst system is a mixture of triethyl lead dihydrogen phosphate and tungsten hexacarbonyl.
Claim 11
Dependent Claim
58 words
The method of claim 6 wherein the reaction takes place at between about 0° and 100°C and at between about 1 and 100 atmospheres and wherein each of a. molybdenum hexacarbonyl or the tungsten hexacarbonyl, or the mixture thereof, and b. the organolead compound comprises about 0.01 to 10% based on the weight of the total reaction mixture.
Claim 12
Dependent Claim
41 words
The method of claim 6 wherein at least one of the organic groups bonded to the lead is substituted by a halogen atom or a hydroxy, nitro, nitroso, methoxy, C 1 -C 12 alkoxy, amino, carboxyl, ester, amide, or nitrile group.
References Cited (Backward Citations)
DE1150060B
Cited
US3489775A
Cited
US3778451A
Cited
US3597459A
Cited
US3654317A
Cited
FR2082811A5
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1979-04-27 | 1979-10-27 | 1980-04-27 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-04-27 | 1983-10-27 | 1984-04-27 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-04-27 | 1987-10-27 | 1988-04-27 | $7700.00 | Window Closed / Lapsed |