GB625909A - Manufacture of polyhydroxy compounds - Google Patents
Manufacture of polyhydroxy compoundsInfo
- Publication number
- GB625909A GB625909A GB24122/46A GB2412246A GB625909A GB 625909 A GB625909 A GB 625909A GB 24122/46 A GB24122/46 A GB 24122/46A GB 2412246 A GB2412246 A GB 2412246A GB 625909 A GB625909 A GB 625909A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mixture
- pressure
- atmospheres
- hydrogen
- carbon monoxide
- 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
- 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
- C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
- C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Polyhydroxy compounds are produced by reacting a mixture of formaldehyde, carbon monoxide and hydrogen, the formaldehyde being initially present, at a pressure of not less than 200 atmospheres and at a temperature of from 80 to 300 DEG C. in the presence of a hydrogenating catalyst. Instead of formaldehyde compounds yielding it under the reaction conditions may be used, e.g. paraformaldehyde, reactive formals, trioxane, and N-methylol derivatives. The reaction products may be further treated with hydrogen to obtain increased yields of hydroxy compounds boiling in the range of the lower glycols, and glycerine. This subsequent hydrogenation may be conducted in the presence of a hydrogenation catalyst, e.g. copper chromite at superatmospheric pressure at a temperature of about 100 DEG to 300 DEG C. Specified hydrogenating catalysts for the main reaction are nickel, cobalt, manganese, iron, chromium, copper, platinum, molybdenum, palladium, zinc, cadmium, ruthenium and compounds thereof or combinations of these materials with each other or with inert supports, e.g. kieselguhr, pumice, or with promoters such as thoria and manganese. Preferred catalysts are cobalt-containing catalysts such as metallic cobalt, reduced sintered cobalt oxide, cobalt carbonyl and salts of cobalt. Preferred temperatures are 100 DEG to 200 DEG C. and pressures of 200 to 1500 atmospheres are preferred. The reaction may be effected in an inert reaction medium, e.g. an aliphatic ether or ester. In examples: (1) a mixture of paraformaldehyde, methyl formate and reduced sintered cobalt oxide is heated in a silver-lined shaker tube under a pressure of 500 to 700 atmospheres of a mixture of carbon monoxide and hydrogen, distillation of the resulting mixture yields a mixture of polyhydroxy compounds; (2) reaction is effected as in (1) but a pressure of 460 to 750 atmospheres is employed, the resulting product is freed from methyl formate and then hydrogenated in methanol solution in the presence of copper chromite at a temperature of 230 DEG C. under a pressure of 745 to 750 atmospheres. Distillation of the product yields fractions containing ethylene glycol and glycerol respectively; (3) a mixture of trioxane, distilled water and reduced sintered cobalt oxide are heated under a pressure of 550 to 640 atmospheres of a gas containing carbon monoxide and hydrogen and the resulting product distilled yielding polyhydroxy compounds; (4) a mixture of paraformaldehyde, methyl formate, and reduced sintered cobalt oxide is heated under pressure and a mixture of carbon monoxide and hydrogen is then injected and the heating continued under a pressure of 445 to 735 atmospheres. Distillation of the product gives a syrupy residue containing polyhydroxy compounds and unspecified oxygenated compounds. The molecular ratio of carbon monoxide to hydrogen used is preferably from 4 : 1 to 1 : 10 and in the examples about 1.5 to 2 moles of carbon monoxide is initially present per mole of formaldehyde.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB24122/46A GB625909A (en) | 1946-08-14 | 1946-08-14 | Manufacture of polyhydroxy compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB24122/46A GB625909A (en) | 1946-08-14 | 1946-08-14 | Manufacture of polyhydroxy compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB625909A true GB625909A (en) | 1949-07-06 |
Family
ID=10206739
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24122/46A Expired GB625909A (en) | 1946-08-14 | 1946-08-14 | Manufacture of polyhydroxy compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB625909A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2757202A (en) * | 1952-03-22 | 1956-07-31 | Exxon Research Engineering Co | Aldehyde synthesis process |
FR2375172A1 (en) * | 1976-10-21 | 1978-07-21 | Chevron Res | Catalytic prepn. of ethylene glycol from formaldehyde - with carbon monoxide and hydrogen using a rhodium cpd. catalyst |
US4533774A (en) * | 1982-11-27 | 1985-08-06 | The British Petroleum Company P.L.C. | Process for the production of ethylene glycol |
-
1946
- 1946-08-14 GB GB24122/46A patent/GB625909A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2757202A (en) * | 1952-03-22 | 1956-07-31 | Exxon Research Engineering Co | Aldehyde synthesis process |
FR2375172A1 (en) * | 1976-10-21 | 1978-07-21 | Chevron Res | Catalytic prepn. of ethylene glycol from formaldehyde - with carbon monoxide and hydrogen using a rhodium cpd. catalyst |
US4533774A (en) * | 1982-11-27 | 1985-08-06 | The British Petroleum Company P.L.C. | Process for the production of ethylene glycol |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2437600A (en) | Synthesis of aldehydes | |
US4064145A (en) | Production of tetrahydrofuran | |
US2451333A (en) | Synthesis of polyhydroxy compounds | |
Covert et al. | The use of nickel as a catalyst for hydrogenation. II | |
Wozniak et al. | Rhenium-catalyzed deoxydehydration of renewable triols derived from sugars | |
US2429878A (en) | Synthesis of glycol ethers | |
US2449470A (en) | Synthesis of organic oxygen | |
CA2048132C (en) | Process for making 1,3-diols from epoxides | |
US2402133A (en) | Manufacture of acrolein | |
KR102313934B1 (en) | Preparation of BDO via hydroformylation of allyl alcohol with glycerin | |
GB625909A (en) | Manufacture of polyhydroxy compounds | |
US2473995A (en) | Synthesis of diethyl ketone | |
KR101060390B1 (en) | Hydrogenation Method of Aldehyde and Apparatus Used Thereof | |
AU604045B2 (en) | Process for making 1,3-glycols from epoxides | |
US2549454A (en) | Preparation of methyl 4-oxobutyrate | |
US2130501A (en) | Reduction of cyclic ethers | |
US4935554A (en) | Process for making 1,3-diols from epoxides | |
JPS62116536A (en) | Production of glycol aldehyde | |
US3404188A (en) | Process for the preparation of polyhydric alcohols | |
US3159653A (en) | Hydroformylation of dihydropyrans | |
US5099073A (en) | Catalytic process for the production of diketone derivatives of polyoxypropylene glycols | |
US2357479A (en) | Hydrogenation of alkoxy-substituted esters and products | |
KR830002563B1 (en) | Process for preparing tetrahydrofuran | |
US2405936A (en) | Formic acid esters | |
GB715744A (en) | Improvements in or relating to the production of aldehydes and acetals |