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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165369Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 15718670, compound

https://huagongshe.com/reaction/2165369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 15718669HCID 15718669—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 15718670HCID 15718670—

Reaction Steps

106 mg (0.5mM) of the product of Step 3, above, in 5 ml of absolute THF is cooled to -78°. 0.328 ml (0.525mM) of 1.6M n-butyllithium in hexane is added and the mixture stirred for 1 hour whilst allowing the temperature to rise to 0°. The mixture is then re-cooled to -60° and 97mg (0.55mM) of benzenesulfonyl chloride is added. After allowing to warm to RT overnight, the mixture is quenched with aqueous NaHCO3 and extracted with ethyl acetate. After washing with NaHCO3 the mixture is dried over Na2SO4 and evaporated to dryness. The residue is triturated with ether and the solids produced precipitated and dried to produce the title product of this step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939159
Source datasetuspto-grants-1990_07
ORD IDord-7bf9a39a77764a5fa10848848d52c2f5
Source noteuspto-grants-1990_07