GB1399639A - Process for epoxidizing olefins with hydrogen peroxide - Google Patents
Process for epoxidizing olefins with hydrogen peroxideInfo
- Publication number
- GB1399639A GB1399639A GB3752872A GB3752872A GB1399639A GB 1399639 A GB1399639 A GB 1399639A GB 3752872 A GB3752872 A GB 3752872A GB 3752872 A GB3752872 A GB 3752872A GB 1399639 A GB1399639 A GB 1399639A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- fluorine
- chlorine
- rcx
- aug
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 2
- 150000001336 alkenes Chemical class 0.000 title 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 4
- 229910052731 fluorine Inorganic materials 0.000 abstract 4
- 239000011737 fluorine Substances 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000006735 epoxidation reaction Methods 0.000 abstract 2
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical compound C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 abstract 2
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 abstract 1
- RMXNSQWYMVTLEU-UHFFFAOYSA-N 2,6-bis(prop-2-enyl)phenol Chemical compound OC1=C(CC=C)C=CC=C1CC=C RMXNSQWYMVTLEU-UHFFFAOYSA-N 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- -1 ketone hydrates Chemical class 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- PJANXHGTPQOBST-UHFFFAOYSA-N trans-Stilbene Natural products C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/19—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic hydroperoxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/12—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with hydrogen peroxide or inorganic peroxides or peracids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/14—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by free hydroxyl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/28—Ethers with hydroxy compounds containing oxirane rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Epoxy Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17173471A | 1971-08-13 | 1971-08-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1399639A true GB1399639A (en) | 1975-07-02 |
Family
ID=22624929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3752872A Expired GB1399639A (en) | 1971-08-13 | 1972-08-11 | Process for epoxidizing olefins with hydrogen peroxide |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS5711905B2 (enrdf_load_stackoverflow) |
| BE (1) | BE787169A (enrdf_load_stackoverflow) |
| DE (1) | DE2239681C3 (enrdf_load_stackoverflow) |
| FR (1) | FR2149428B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1399639A (enrdf_load_stackoverflow) |
| IT (1) | IT963971B (enrdf_load_stackoverflow) |
| NL (1) | NL7211070A (enrdf_load_stackoverflow) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4344887A (en) | 1979-12-28 | 1982-08-17 | General Electric Company | Method for epoxidizing olefins |
| US4389529A (en) | 1981-05-15 | 1983-06-21 | General Electric Company | Method for epoxidizing olefins |
| US4410715A (en) | 1982-07-14 | 1983-10-18 | Exxon Research & Engineering Co. | Process for the epoxidation of olefins using a group V metal co-catalyst I and a phenolic hydrocarbon co-catalyst II |
| US4418203A (en) | 1981-12-21 | 1983-11-29 | Shell Oil Company | Process for the epoxidation of olefins |
| EP0096130A1 (en) * | 1982-06-11 | 1983-12-21 | Exxon Research And Engineering Company | Process for the epoxidation of olefins |
| CN104803951A (zh) * | 2015-05-15 | 2015-07-29 | 南京工业大学 | 一种采用微流场反应技术制备高品质环氧环己烷的方法 |
| CN106660978A (zh) * | 2014-08-27 | 2017-05-10 | 沙特基础工业全球技术有限公司 | 2‑(2,3‑环氧丙基)苯酚组合物及制备方法 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE863237A (fr) * | 1977-02-01 | 1978-07-24 | Ugine Kuhlmann | Procede d'epoxydation catalytique des olefines |
| FR2423486A1 (fr) * | 1978-04-19 | 1979-11-16 | Roussel Uclaf | Nouveau reactif d'epoxydation |
| DE3722486A1 (de) * | 1987-07-03 | 1989-01-12 | Schering Ag | Neues epoxidierungs-reagenz und seine verwendung |
| JP5300218B2 (ja) * | 2006-06-23 | 2013-09-25 | キヤノン株式会社 | 微細構造体、その製造方法および液体吐出ヘッド |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2786854A (en) * | 1957-03-26 | Process of making oxirane compounds |
-
0
- BE BE787169D patent/BE787169A/nl unknown
-
1972
- 1972-08-11 IT IT2816572A patent/IT963971B/it active
- 1972-08-11 GB GB3752872A patent/GB1399639A/en not_active Expired
- 1972-08-11 JP JP8003072A patent/JPS5711905B2/ja not_active Expired
- 1972-08-11 DE DE19722239681 patent/DE2239681C3/de not_active Expired
- 1972-08-11 FR FR7229054A patent/FR2149428B1/fr not_active Expired
- 1972-08-14 NL NL7211070A patent/NL7211070A/xx not_active Application Discontinuation
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4344887A (en) | 1979-12-28 | 1982-08-17 | General Electric Company | Method for epoxidizing olefins |
| US4389529A (en) | 1981-05-15 | 1983-06-21 | General Electric Company | Method for epoxidizing olefins |
| US4418203A (en) | 1981-12-21 | 1983-11-29 | Shell Oil Company | Process for the epoxidation of olefins |
| EP0096130A1 (en) * | 1982-06-11 | 1983-12-21 | Exxon Research And Engineering Company | Process for the epoxidation of olefins |
| US4410715A (en) | 1982-07-14 | 1983-10-18 | Exxon Research & Engineering Co. | Process for the epoxidation of olefins using a group V metal co-catalyst I and a phenolic hydrocarbon co-catalyst II |
| CN106660978A (zh) * | 2014-08-27 | 2017-05-10 | 沙特基础工业全球技术有限公司 | 2‑(2,3‑环氧丙基)苯酚组合物及制备方法 |
| EP3186235A4 (en) * | 2014-08-27 | 2018-04-25 | SABIC Global Technologies B.V. | 2-(2,3-epoxypropyl)phenol composition and method of making |
| US10214503B2 (en) | 2014-08-27 | 2019-02-26 | Sabic Global Technologies B.V. | 2-(2,3-epdxypropyl)phenol composition and method of making |
| CN104803951A (zh) * | 2015-05-15 | 2015-07-29 | 南京工业大学 | 一种采用微流场反应技术制备高品质环氧环己烷的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2149428A1 (enrdf_load_stackoverflow) | 1973-03-30 |
| DE2239681B2 (de) | 1981-02-26 |
| NL7211070A (enrdf_load_stackoverflow) | 1973-02-15 |
| JPS5711905B2 (enrdf_load_stackoverflow) | 1982-03-08 |
| JPS4828403A (enrdf_load_stackoverflow) | 1973-04-14 |
| BE787169A (nl) | 1973-02-05 |
| FR2149428B1 (enrdf_load_stackoverflow) | 1974-10-04 |
| IT963971B (it) | 1974-01-21 |
| DE2239681A1 (de) | 1973-02-22 |
| DE2239681C3 (de) | 1981-12-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |