GB916751A - Preparation of sulphinic acids - Google Patents
Preparation of sulphinic acidsInfo
- Publication number
- GB916751A GB916751A GB2376060A GB2376060A GB916751A GB 916751 A GB916751 A GB 916751A GB 2376060 A GB2376060 A GB 2376060A GB 2376060 A GB2376060 A GB 2376060A GB 916751 A GB916751 A GB 916751A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphur dioxide
- aluminium compound
- sulphinic
- acid
- solvent
- 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
- C07C313/00—Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C313/02—Sulfinic acids; Derivatives thereof
- C07C313/04—Sulfinic acids; Esters thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Sulphinic acids are prepared by reacting a trialkyl or aryl aluminium compound with sulphur dioxide, the aluminium compound being added to the sulphur dioxide at a temperature varying from -75 to 50 DEG C. in the presence of a solvent for the sulphur dioxide, the solvent forming a coordination complex with the aluminium compound and having a boiling-point above the reaction temperature employed, hydrolysing the resulting reaction product with water or an acid, and recovering the sulphinic acid from the hydrolysate. Suitable solvents are, for example, tetrahydrofuran, pyridine, triethylamine, dimethylformamide, dimethyl acetamide, diethylformamide, dimethyl propionamide, anisole, diphenyl ether, dimethyl aniline, N-methyl pyrrole, N-ethyl pyrrole, trimethylamine, dibenzofuran, quinoline and diethylaniline. The sulphinic acid may be present in the hydrolysate in the aqueous phase or as an organic phase according to its solubility. If present in the aqueous phase it may be separated by solvent extraction. Specifications 819,181 and 916,752 are referred to.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US82773359A | 1959-07-17 | 1959-07-17 | |
US3179260A | 1960-06-14 | 1960-06-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB916751A true GB916751A (en) | 1963-01-30 |
Family
ID=26707610
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2376060A Expired GB916751A (en) | 1959-07-17 | 1960-07-07 | Preparation of sulphinic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB916751A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102731349A (en) * | 2011-04-08 | 2012-10-17 | 中国中化股份有限公司 | Aromatic sulfinic acid compound preparation method |
-
1960
- 1960-07-07 GB GB2376060A patent/GB916751A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102731349A (en) * | 2011-04-08 | 2012-10-17 | 中国中化股份有限公司 | Aromatic sulfinic acid compound preparation method |
CN102731349B (en) * | 2011-04-08 | 2013-12-18 | 中国中化股份有限公司 | Aromatic sulfinic acid compound preparation method |
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