GB1124320A - Production of glycidol and glycerine - Google Patents
Production of glycidol and glycerineInfo
- Publication number
- GB1124320A GB1124320A GB16824/68A GB1682468A GB1124320A GB 1124320 A GB1124320 A GB 1124320A GB 16824/68 A GB16824/68 A GB 16824/68A GB 1682468 A GB1682468 A GB 1682468A GB 1124320 A GB1124320 A GB 1124320A
- Authority
- GB
- United Kingdom
- Prior art keywords
- epoxidation
- hydroperoxide
- glycidol
- allyl alcohol
- glycerine
- 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
Abstract
Glycidol is prepared by epoxidizing propylene to propylene oxide by reaction with an organic hydroperoxide in the liquid phase and in the presence of a metal epoxidation catalyst, isomerizing the propylene oxide to allyl alcohol and epoxidizing allyl alcohol to glycidol by reaction with an organic hydroperoxide in the liquid phase in the presence of a metal epoxidation catalyst. The glycidol may be hydrolysed to glycerine, e.g. with water at 20-200 DEG C. in the presence of an acidic or basic catalyst. Specified epoxidation catalysts are compounds of Ti, V, Cr, Se, Zr, Nb, Te, Mo, Ta, W, Re and U. Vanadium catalysts are preferred, especially for the epoxidation of allyl alcohol. The preferred hydroperoxide is a -phenylethyl hydroperoxide. The two epoxidation reactions may be effected simultaneously. The combined effluents from the epoxidation stages may be treated for the recovery of the alcohol corresponding to the hydroperoxide; acetophenone may also be recovered when a -phenylethyl hydroperoxide is used.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40995864A | 1964-11-09 | 1964-11-09 | |
US41956864A | 1964-12-18 | 1964-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1124320A true GB1124320A (en) | 1968-08-21 |
Family
ID=27020815
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16824/68A Expired GB1124320A (en) | 1964-11-09 | 1965-11-03 | Production of glycidol and glycerine |
GB46610/65A Expired GB1124065A (en) | 1964-11-09 | 1965-11-03 | Production of glycidol and glycerine |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB46610/65A Expired GB1124065A (en) | 1964-11-09 | 1965-11-03 | Production of glycidol and glycerine |
Country Status (10)
Country | Link |
---|---|
BE (1) | BE671382A (en) |
BR (1) | BR6574622D0 (en) |
CH (1) | CH447136A (en) |
DE (1) | DE1543026A1 (en) |
ES (1) | ES319382A1 (en) |
FR (1) | FR1462491A (en) |
GB (2) | GB1124320A (en) |
IL (1) | IL24594A (en) |
NL (1) | NL6513621A (en) |
SE (1) | SE337583B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3374153A (en) * | 1966-07-25 | 1968-03-19 | Halcon International Inc | Process for recovery of glycidol from alcohol by azeotropic distillation with a hydrocarbon |
JP2686975B2 (en) * | 1987-09-14 | 1997-12-08 | アルコ・ケミカル・カンパニー | Collection method of chiral epoxy alcohol in asymmetric epoxidation method |
-
1965
- 1965-10-21 NL NL6513621A patent/NL6513621A/xx unknown
- 1965-10-25 BE BE671382D patent/BE671382A/xx unknown
- 1965-11-03 GB GB16824/68A patent/GB1124320A/en not_active Expired
- 1965-11-03 GB GB46610/65A patent/GB1124065A/en not_active Expired
- 1965-11-05 BR BR174622/65A patent/BR6574622D0/en unknown
- 1965-11-08 IL IL24594A patent/IL24594A/en unknown
- 1965-11-08 FR FR37589A patent/FR1462491A/en not_active Expired
- 1965-11-09 CH CH1542765A patent/CH447136A/en unknown
- 1965-11-09 DE DE19651543026 patent/DE1543026A1/en not_active Withdrawn
- 1965-11-09 SE SE14435/65A patent/SE337583B/xx unknown
- 1965-11-09 ES ES0319382A patent/ES319382A1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1543026A1 (en) | 1969-09-11 |
GB1124065A (en) | 1968-08-21 |
IL24594A (en) | 1969-11-12 |
BE671382A (en) | 1966-04-25 |
NL6513621A (en) | 1966-05-10 |
BR6574622D0 (en) | 1973-08-14 |
ES319382A1 (en) | 1966-05-01 |
CH447136A (en) | 1967-11-30 |
SE337583B (en) | 1971-08-16 |
FR1462491A (en) | 1966-04-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FR2217372A1 (en) | Low mol wt polyglycidyl ethers prepn. - by catalytic etherification of polyvalent phenols with epihalohydrins | |
GB1420662A (en) | Process for the splitting by oxidation of unsaturated hydro carbons | |
ES378130A1 (en) | A process for epoxidizing olefins with organic hydroperoxides | |
ES395527A1 (en) | Catalyst for producing oxirane compounds by epoxidizing olefins with hydroperoxides | |
GB1016900A (en) | Oxidation of olefins to epoxy-alcohols | |
GB1124320A (en) | Production of glycidol and glycerine | |
IE35397B1 (en) | A process for epoxidizing olefins with hydroperoxides for producing oxirane compounds | |
GB1128150A (en) | Oxidation of ethylbenzene | |
GB1102005A (en) | Process for the catalytic liquid phase dehydrogenation of cyclododecanol | |
ES347524A1 (en) | Process for preparing oxirane compound | |
US5103027A (en) | Olefin expoxidation using an oxorhenium porphyrin complex catalyst and an organic hydroperoxide | |
GB1133313A (en) | Production of styrenes and of oxirane compounds | |
CN108993616B (en) | Regeneration method of phosphomolybdic/tungstic heteropoly acid quaternary ammonium salt catalyst | |
ES348828A1 (en) | Epoxidation of olefinically unsaturated compounds | |
GB1115220A (en) | Production of oxirane compounds | |
GB1104821A (en) | Epoxidation of olefinically unsaturated compounds | |
NL7504156A (en) | Glycidol from allyl alcohol - by epoxidation using hydroperoxide with vanadium compound catalyst | |
DK134437B (en) | Process for the selective decomposition of unconverted organic hydroperoxide in the effluent from an epoxidation reaction in which an olefinic compound is converted to an oxirane compound by the action of an organic hydroperoxide. | |
Finnegan et al. | The epoxidation of 3-methylcyclopentene: An unexpected conformational effect | |
GB1308340A (en) | Production of oxirane compounds | |
EP0151289A3 (en) | Process for the preparation of oxiranes | |
GB1074330A (en) | Epoxidation of olefinically unsaturated compounds | |
NL7513858A (en) | Simultaneous prodn of alkene peroxides and styrene derivs - by epoxidn of 3-4C alkenes with alkyl aryl hydroperoxides using niobium or tantalum cpd catalyst | |
NL6514129A (en) | ||
SU456631A1 (en) | Method of preparing catalyst for epoxidation of olefinic hydrocarbons |