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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006719Generated: October 31, 2026

4-Fluorobenzenesulfonyl chloride → Sodium 4-fluorobenzene sulfinate

https://huagongshe.com/reaction/1006719

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 numberUS06790978B2
Source datasetuspto-grants-2004_09
ORD IDord-ad20ef8cd63848ac9f213257112838ae
Source noteuspto-grants-2004_09