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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359164Generated: November 2, 2026

4-Fluorobenzenesulfonyl chloride → Sodium 4-fluorobenzene sulfinate

https://huagongshe.com/reaction/1359164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
ProductSodium 4-fluorobenzene sulfinateHCID 421250—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-fluorobenzenesulfonyl chloride (2 g, 10.28 mmol) in 50 mL of THF (distilled from Na-benzophenone) is cooled to 0+ C. and sodium borohydride (1.9 g, 51.4 mmol) is added portionwise. The reaction is stirred at 0° C. for 2 h, then warmed to RT, and after 2 h, quenched with water (5 mL). The solvent is evaporated and the aqueous residue is acidified by addition of aqueous 6N HCl. The product is taken up in EtOAc, washed with brine, dried over anhydrous Na2SO4 and concentrated to give 4-fluorobenzenesulfinic acid: NMR (DMSO-d6) 7.12 (app t, 2H, J=8.3), 7.5 (dd, 2H, J=8.3, 6); ESI-MS 159 [M−1]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599942B1
Source datasetuspto-grants-2003_07
ORD IDord-10c8b18a6e594cc2b39cf46c301c8b7e
Source noteuspto-grants-2003_07