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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282446Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 9862505, compound

https://huagongshe.com/reaction/1282446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant5-Hydroxybenzo[b]thiophene-3-carboxylic acidHCID 11412897—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 9862505HCID 986250596.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455741B1
Source datasetuspto-grants-2002_09
ORD IDord-2a8e64f9fd524b988f0d710249f63955
Source noteuspto-grants-2002_09