HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040399Generated: October 25, 2026
Thionyl Chloride → o-Formylbenzenesulfonyl chloride
https://huagongshe.com/reaction/1040399
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | CID 53445294 | HCID 53445294 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | o-Formylbenzenesulfonyl chloride | HCID 30723 | 38.2% |
Reaction Steps
To a solution of 2-sulfobenzaldehyde sodium salt (2.0 g, 9.6 mmol) in 0.8 mL of dry N,N-dimethylformamide was added thionyl chloride (7.0 mL, 96 mmol) under nitrogen at 0° C. After being stirred at 100° C. for 3 min, the reaction mixture was diluted with diethyl ether and water at 0° C., successively. The separated organic layer was washed with water, brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo to obtain crude 2-formylbenzenesulfonyl chloride (0.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552220B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-35c65136408f4fcb9a232a99cddef21d |
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| Source note | uspto-grants-2013_10 |
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