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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282432Generated: November 1, 2026

4-Chlorobenzenesulfonyl chloride → HCID 18424427, compound

https://huagongshe.com/reaction/1282432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantSodium hydrideHCID 24758—
Reactant1-Fluoro-2-fluoromethyl-3-butyn-2-olHCID 18424428—
ReactantHCID 21921625HCID 21921625—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18424427HCID 1842442775%

Reaction Steps

An amount (1.2 g) of 1-fluoro-2-fluoromethyl-3-butyn-2-ol and p-chlorobenzenesulfonyl chloride (2.1 g) were dissolved in tetrahydrofuran (10 ml); to the solution under cooling with ice, 60% oily sodium hydride (0.48 g) was added under a nitrogen atmosphere. After the end of the addition, the mixture was stirred for 4 hours while its temperature was raised to room temperature. A hexane/ethane mixed solvent (1/1) was added to the reaction mixture, which was then washed with water and a saturated aqueous solution of sodium chloride, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (eluent; hexane/methylene chloride=1/1) and then recrystallized from methylene chloride/hexane to give the titled compound (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455708B1
Source datasetuspto-grants-2002_09
ORD IDord-e85547b9b0774313a6024f9ccff191b6
Source noteuspto-grants-2002_09