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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193504Generated: November 3, 2026

Ethenesulfonyl chloride, 2-phenyl- → HCID 3087418, compound

https://huagongshe.com/reaction/1193504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthenesulfonyl chloride, 2-phenyl-HCID 107500—
Reactant5-Ethoxy-2-pyrrolidinoneHCID 3580555—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 3087418HCID 308741822%

Reaction Conditions

Temperature-5 °C

Reaction Steps

2.6 g of 2-oxo-5-ethoxy pyrrolidine is dissolved in 80 cm3 of anhydrous tetrahydrofuran, then cooled to -5° C., and 12.6 cm3 of butyllithium is added. After 20 minutes under agitation, there is added slowly at the same temperature, 4.05 g of styrene-sulphonyl chloride (CA 47, 3262c (1953)) in 10 cm3 of tetrahydrofuran. After allowing this to return to ambient temperature, after 4 hours, it is concentrated to dryness and the residue is chromatographed on silica. 1.3 g of the expected product is obtained, which is crystallized from a mixture of ethyl ether and hexane. m.p.=61°-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810722
Source datasetuspto-grants-1989_03
ORD IDord-29368e2b03694131b0ca3aa0ddf59d92
Source noteuspto-grants-1989_03