GB1143433A - Epoxidation of unsaturated hydrocarbons containing at least one olefinic double bond - Google Patents
Epoxidation of unsaturated hydrocarbons containing at least one olefinic double bondInfo
- Publication number
- GB1143433A GB1143433A GB1644666A GB1644666A GB1143433A GB 1143433 A GB1143433 A GB 1143433A GB 1644666 A GB1644666 A GB 1644666A GB 1644666 A GB1644666 A GB 1644666A GB 1143433 A GB1143433 A GB 1143433A
- Authority
- GB
- United Kingdom
- Prior art keywords
- double bond
- resin
- unsaturated hydrocarbons
- epoxides
- april
- 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
- 238000006735 epoxidation reaction Methods 0.000 title abstract 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 title abstract 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 abstract 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 abstract 2
- 150000002118 epoxides Chemical class 0.000 abstract 2
- 239000007791 liquid phase Substances 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 abstract 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 abstract 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 abstract 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 abstract 1
- 239000001768 carboxy methyl cellulose Substances 0.000 abstract 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 abstract 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 abstract 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 abstract 1
- 229940105329 carboxymethylcellulose Drugs 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003729 cation exchange resin Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 150000004292 cyclic ethers Chemical class 0.000 abstract 1
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 abstract 1
- 239000004913 cyclooctene Substances 0.000 abstract 1
- 238000000354 decomposition reaction Methods 0.000 abstract 1
- -1 diallylbenzene Natural products 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 abstract 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 abstract 1
- 238000005502 peroxidation Methods 0.000 abstract 1
- 150000007965 phenolic acids Chemical class 0.000 abstract 1
- 239000002798 polar solvent Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 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
- 239000011541 reaction mixture Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- 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
- 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
- C07D301/14—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic peracids, or salts, anhydrides or esters thereof
- C07D301/16—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic peracids, or salts, anhydrides or esters thereof formed in situ, e.g. from carboxylic acids and hydrogen peroxide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Epoxy Compounds (AREA)
- Epoxy Resins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR13526A FR1440125A (fr) | 1965-04-16 | 1965-04-16 | Nouveau procédé d'époxydation des oléfines en phase liquide par l'eau oxygénée |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1143433A true GB1143433A (en) | 1969-02-19 |
Family
ID=8576603
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1644666A Expired GB1143433A (en) | 1965-04-16 | 1966-04-14 | Epoxidation of unsaturated hydrocarbons containing at least one olefinic double bond |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE678542A (cs) |
| DE (1) | DE1593355A1 (cs) |
| FR (1) | FR1440125A (cs) |
| GB (1) | GB1143433A (cs) |
| LU (1) | LU50905A1 (cs) |
| NL (1) | NL6605134A (cs) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| EP0190609A3 (en) * | 1985-02-05 | 1987-06-16 | Enichem Sintesi S.P.A. | Process for the monoepoxidation of compounds containing two double bonds |
| CN112028858A (zh) * | 2020-09-11 | 2020-12-04 | 中国天辰工程有限公司 | 一种环氧环己烷的合成方法 |
| CN112047904A (zh) * | 2020-09-11 | 2020-12-08 | 中国天辰工程有限公司 | 一种利用微通道反应器制备环氧环己烷的方法 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19505858A1 (de) * | 1995-02-21 | 1996-10-31 | Basf Ag | Verfahren zur Herstellung von Epoxiden mittels aromatischer Peroxycarbonsäuren |
| FR2810980B1 (fr) * | 2000-06-28 | 2004-05-21 | Solvay | Procede de fabrication d'oxiranne en presence d'un catalyseur sous forme de particules |
-
1965
- 1965-04-16 FR FR13526A patent/FR1440125A/fr not_active Expired
-
1966
- 1966-03-28 BE BE678542D patent/BE678542A/xx unknown
- 1966-04-14 DE DE19661593355 patent/DE1593355A1/de active Pending
- 1966-04-14 GB GB1644666A patent/GB1143433A/en not_active Expired
- 1966-04-15 LU LU50905A patent/LU50905A1/xx unknown
- 1966-04-15 NL NL6605134A patent/NL6605134A/xx unknown
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| EP0190609A3 (en) * | 1985-02-05 | 1987-06-16 | Enichem Sintesi S.P.A. | Process for the monoepoxidation of compounds containing two double bonds |
| CN112028858A (zh) * | 2020-09-11 | 2020-12-04 | 中国天辰工程有限公司 | 一种环氧环己烷的合成方法 |
| CN112047904A (zh) * | 2020-09-11 | 2020-12-08 | 中国天辰工程有限公司 | 一种利用微通道反应器制备环氧环己烷的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1440125A (fr) | 1966-05-27 |
| LU50905A1 (cs) | 1966-06-15 |
| BE678542A (cs) | 1966-09-01 |
| DE1593355A1 (de) | 1971-02-25 |
| NL6605134A (cs) | 1966-10-17 |
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