ES395616A1 - Method for the epoxidation of ethylene - Google Patents
Method for the epoxidation of ethyleneInfo
- Publication number
- ES395616A1 ES395616A1 ES395616A ES395616A ES395616A1 ES 395616 A1 ES395616 A1 ES 395616A1 ES 395616 A ES395616 A ES 395616A ES 395616 A ES395616 A ES 395616A ES 395616 A1 ES395616 A1 ES 395616A1
- Authority
- ES
- Spain
- Prior art keywords
- ethylene
- solvent
- epoxidation
- hydroperoxide
- reaction
- 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
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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Epoxy Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A method for the epoxidation of ethylene by reaction of ethylene with tert-butyl hydroperoxide, in the presence of a molybdenum catalyst and a solvent, characterized in that the solvent is benzene, an alkylated benzene of 1 to 6 carbon atoms in the portion alkyl or a saturated alkane containing 7 to 14 carbon atoms and because the reaction is carried out between 80º and 115ºC, with an ethylene to hydroperoxide molar ratio of between 5: 1 and 20: 1 and a solvent to hydroperoxide molar ratio between 12: 1 and 25: 1. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9538070A | 1970-12-04 | 1970-12-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES395616A1 true ES395616A1 (en) | 1973-11-16 |
Family
ID=22251689
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES395616A Expired ES395616A1 (en) | 1970-12-04 | 1971-09-30 | Method for the epoxidation of ethylene |
Country Status (8)
Country | Link |
---|---|
BE (1) | BE773865A (en) |
CA (1) | CA967582A (en) |
DE (1) | DE2148432A1 (en) |
ES (1) | ES395616A1 (en) |
FR (1) | FR2111317A5 (en) |
GB (1) | GB1337296A (en) |
IT (1) | IT939572B (en) |
NL (1) | NL7114023A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5290527A (en) * | 1992-11-05 | 1994-03-01 | Texaco Chemical Company | Molybdenum recovery |
US5274138A (en) * | 1993-01-21 | 1993-12-28 | Texaco Chemical Company | Epoxidation process for manufacture of olefin oxide and alcohol |
US5539131A (en) * | 1995-07-13 | 1996-07-23 | Arco Chemical Technology, L.P. | Olefin epoxidation process |
-
1971
- 1971-09-08 CA CA122,354A patent/CA967582A/en not_active Expired
- 1971-09-28 DE DE19712148432 patent/DE2148432A1/de active Pending
- 1971-09-28 GB GB4515171A patent/GB1337296A/en not_active Expired
- 1971-09-30 ES ES395616A patent/ES395616A1/en not_active Expired
- 1971-10-12 NL NL7114023A patent/NL7114023A/xx not_active Application Discontinuation
- 1971-10-13 BE BE773865A patent/BE773865A/en unknown
- 1971-10-13 FR FR7136792A patent/FR2111317A5/fr not_active Expired
- 1971-10-14 IT IT5346871A patent/IT939572B/en active
Also Published As
Publication number | Publication date |
---|---|
BE773865A (en) | 1972-04-13 |
DE2148432A1 (en) | 1972-06-08 |
FR2111317A5 (en) | 1972-06-02 |
NL7114023A (en) | 1972-06-06 |
CA967582A (en) | 1975-05-13 |
IT939572B (en) | 1973-02-10 |
GB1337296A (en) | 1973-11-14 |
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