HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282446Generated: November 1, 2026
Benzenesulfonyl chloride → HCID 9862505, compound
https://huagongshe.com/reaction/1282446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 5-Hydroxybenzo[b]thiophene-3-carboxylic acid | HCID 11412897 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 9862505 | HCID 9862505 | 96.5% |
Reaction Steps
5-Hydroxybenzo[b]thiophene-3-carboxylic acid (11) (M.Martin-Smith et al. J. Chem. Soc (C), 1899-1905 (1967) 8.63 g (44.4 mmol)) was dissolved in aqueous tetrahydrofuran (water content, 20%; 160 ml) and 1 N sodium hydroxide (44 ml). To the solution were added dropwise 0.56 N sodium hydroxide (87 ml) and benzenesulfonyl chloride (6.2 ml, 48.4 mmol) simultaneously with stirring under ice-cooling while maintaining the pH at 11-12. After the completion of the reaction, the mixture was diluted with water, basified, and washed with toluene. The aqueous layer was made slightly acidic by adding concentrated hydrochloric acid with stirring, and the deposited crystals were filtered, washed with water and dried to provide 14.33 g of 5-benzenesulfonyloxybenzo[b]thiophene-3-carboxylic acid (12). M.p. 202-203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455741B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-2a8e64f9fd524b988f0d710249f63955 |
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| Source note | uspto-grants-2002_09 |
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