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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398588Generated: October 28, 2026

Sodium bis(trimethylsilyl)amide → 2-(3-Chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-acrylic acid ethyl ester

https://huagongshe.com/reaction/398588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantEthyl 2-(3-chloro-4-(methylthio)phenyl)-2-oxoacetateHCID 53981255—
ReactantHCID 178506552HCID 178506552—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-acrylic acid ethyl esterHCID 5440521960%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of cyclopentylmethyl triphenylphosphine iodide (725 mg, 1.53 mmol) in tetrahydrofuran (10 mL) was cooled to 0° C. and then treated with a 1.0M solution of sodium bis(trimethylsilyl)amide in tetrahydrofuran (2.14 mL, 2.14 mmol). The resulting red reaction mixture was stirred at 0° C. for 45 minutes and then slowly treated with a solution of (3-chloro-4-methylsulfanyl-phenyl)-oxo-acetic acid ethyl ester (355 mg, 1.37 mmol) in tetrahydrofuran (5 mL). The reaction mixture was warmed to 25° C. where it was stirred for 20 h. The reaction mixture was then diluted with water (50 mL) and extracted with diethyl ether (3×25 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (Flash 12M, Silica, 80/20 hexanes/ethyl acetate) afforded 2-(3-chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-acrylic acid ethyl ester (267 mg, 60%) as a yellow oil consisting of a 2:1 mixture of (E):(Z) isomers. The isomeric mixture was used without further separation and characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-a9ce6ef84d1148eea8b9a2331272f6d1
Source noteuspto-grants-2003_08