GB492726A - Improvements in or relating to the manufacture of ketones and alcohols from olefines - Google Patents
Improvements in or relating to the manufacture of ketones and alcohols from olefinesInfo
- Publication number
- GB492726A GB492726A GB8876/37A GB887637A GB492726A GB 492726 A GB492726 A GB 492726A GB 8876/37 A GB8876/37 A GB 8876/37A GB 887637 A GB887637 A GB 887637A GB 492726 A GB492726 A GB 492726A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali
- mixture
- alcohol
- chlorhydrin
- butene
- 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
- 150000002576 ketones Chemical class 0.000 title abstract 5
- 238000004519 manufacturing process Methods 0.000 title abstract 5
- 150000001298 alcohols Chemical class 0.000 title abstract 3
- 239000003513 alkali Substances 0.000 abstract 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 6
- 125000002947 alkylene group Chemical group 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 4
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 abstract 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 4
- 239000003518 caustics Substances 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 abstract 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 238000005868 electrolysis reaction Methods 0.000 abstract 2
- 238000005984 hydrogenation reaction Methods 0.000 abstract 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 229940032007 methylethyl ketone Drugs 0.000 abstract 2
- 230000003472 neutralizing effect Effects 0.000 abstract 2
- 150000003138 primary alcohols Chemical class 0.000 abstract 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 2
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 abstract 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/64—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by simultaneous introduction of -OH groups and halogens
- C07C29/66—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by simultaneous introduction of -OH groups and halogens by addition of hypohalogenous acids, which may be formed in situ, to carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/30—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with halogen containing compounds, e.g. hypohalogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/56—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds
- C07C45/57—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom
- C07C45/58—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom in three-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR885703X | 1936-03-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB492726A true GB492726A (en) | 1938-09-26 |
Family
ID=9375586
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8876/37A Expired GB492726A (en) | 1936-03-28 | 1937-03-25 | Improvements in or relating to the manufacture of ketones and alcohols from olefines |
| GB27538/38A Expired GB496264A (en) | 1936-03-28 | 1937-03-25 | Improvements in or relating to the hydrogenation of alkylene oxides |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB27538/38A Expired GB496264A (en) | 1936-03-28 | 1937-03-25 | Improvements in or relating to the hydrogenation of alkylene oxides |
Country Status (5)
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2689870A (en) * | 1954-09-21 | Method for the preparation of aryl | ||
| US3009959A (en) * | 1961-11-21 | Figure i | ||
| GB634080A (en) * | 1946-03-29 | 1950-03-15 | John George Mackay Bremner | Improvements in and relating to the hydrogenolysis of 2-alkyl substituted furans |
| US2561984A (en) * | 1949-04-25 | 1951-07-24 | Phillips Petroleum Co | Production of primary alcohols and aldehydes |
| US2727048A (en) * | 1952-11-10 | 1955-12-13 | Charles H Mack | Catalytic hydrogenation of epoxidized olefinic compounds |
| US2769845A (en) * | 1953-04-16 | 1956-11-06 | Olin Mathieson | Production of olefin chlorohydrins |
| DE1080995B (de) * | 1954-06-10 | 1960-05-05 | Exxon Research Engineering Co | Verfahren zur katalytischen Herstellung von aliphatischen Ketonen aus Epoxyden |
| US4590313A (en) * | 1982-06-02 | 1986-05-20 | Atlantic Richfield Company | Method for producing primary alcohols by catalytic hydrogenation of terminal epoxides |
| DE19915894C1 (de) * | 1999-04-08 | 2000-08-24 | Inventa Ag | Verfahren zur Umwandlung von cis- und trans-Cyclododecenoxid in Cyclododecanon |
-
0
- BE BE420819D patent/BE420819A/xx unknown
-
1936
- 1936-03-28 FR FR815494D patent/FR815494A/fr not_active Expired
- 1936-05-15 DE DES5398D patent/DE885703C/de not_active Expired
-
1937
- 1937-03-24 US US132871A patent/US2167203A/en not_active Expired - Lifetime
- 1937-03-25 GB GB8876/37A patent/GB492726A/en not_active Expired
- 1937-03-25 GB GB27538/38A patent/GB496264A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE420819A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| US2167203A (en) | 1939-07-25 |
| GB496264A (en) | 1938-11-25 |
| DE885703C (de) | 1953-08-06 |
| FR815494A (fr) | 1937-07-12 |
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