GB264791A - Manufacture of acetals - Google Patents
Manufacture of acetalsInfo
- Publication number
- GB264791A GB264791A GB25400/26A GB2540026A GB264791A GB 264791 A GB264791 A GB 264791A GB 25400/26 A GB25400/26 A GB 25400/26A GB 2540026 A GB2540026 A GB 2540026A GB 264791 A GB264791 A GB 264791A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- reaction mixture
- reaction
- alcohol
- acetal
- 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
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/30—Compounds having groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
264,791. Consortium fur Elektrochemische Industrie Ges. Jan. 25, 1926, [Convention date]. Addition to 257,622. Acetals; acetaldehyde.-The process of making acetals which consists in treating monohydric or polyhydric alcohols with acetylene in the presence of a mercury salt and continuously removing the acetal produced, as described in the parent Specification, is now modified by using alcohol containing water, which is converted into acetaldehyde. To increase the proportion of acetal in the product, the mixed vapour from the reaction mixture may be partly condensed, and the condensate returned to the reaction mixture, or the products may again be passed through the apparatus several times. The acetaldehyde formed may be fractionated out of the vapours, or removed therefrom by washing, say with the alcohol used in the reaction. A portion of the liquid reaction mixture may be withdrawn continuously or intermittingly, so that mercury sludge may be removed, and the composition of the liquid adjusted; the reaction liquid may be circulated for this purpose. In examples, (1) a suspension of mercury sulphate in ethyl alcohol of 92 per cent strength is heated to about 70‹ C. and acetylene passed in. After condensing out the vapours escaping from the reaction mixture; the unconverted acetylene is returned with the fresh gas. An emulsion of mercury sulphate in the water-contaminated alcohol is added to the reaction mixture; fresh alcohol is also added: (2) the process is conducted as in the preceding example, but in a reaction vessel with a, fractionating apparatus so that a part of the vapour distilling is condensed and returned to the reaction vessel. The product may contain 40 per cent or more of acetal and 15 per cent of aldehyde; (3,) the product from Example (2) is again passed through the reaction apparatus, using a more concentrated emulsion. A product containing 62 per cent acetal and 16 per cent aldehyde may thus be obtained.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE264791X | 1926-01-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB264791A true GB264791A (en) | 1927-05-12 |
Family
ID=5991157
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB25400/26A Expired GB264791A (en) | 1926-01-25 | 1926-10-12 | Manufacture of acetals |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB264791A (en) |
-
1926
- 1926-10-12 GB GB25400/26A patent/GB264791A/en not_active Expired
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