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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196713Generated: October 28, 2026

Methanesulfonyl chloride → HCID 131717378, compound

https://huagongshe.com/reaction/1196713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 15078318HCID 15078318—
ReactantEthyl acetate hexaneHCID 21226206—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 131717378HCID 131717378—

Reaction Steps

Methanesulfonyl chloride (0.097 mL, 1.25 mmol) was added to a solution of trans-2-[3-(2-hydroxyethylsulfonyl)-4,5-di-n-propoxyphenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran (338 mg, 0.63 mmol) in dichloromethane (3 mL) and pyridine (1.3 mL). The reaction mixture was stirred at room temperature for 2 h, and worked-up as usual to give a syrup, Rf 0.52 (hexane-ethyl acetate; 1:2 v/v). This material was used directly in the next experiment without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114961
Source datasetuspto-grants-1992_05
ORD IDord-7d60563fc02e49918cbf64423b021ab9
Source noteuspto-grants-1992_05