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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398552Generated: October 29, 2026

3-Cyclopentyl-2-(4-ethanesulfonyl-phenyl)-acrylic acid ethyl ester → 3-Cyclopentyl-2-(4-ethanesulfonyl-phenyl)-propionic acid ethyl ester

https://huagongshe.com/reaction/398552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyl-2-(4-ethanesulfonyl-phenyl)-acrylic acid ethyl esterHCID 53813064—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-Cyclopentyl-2-(4-ethanesulfonyl-phenyl)-propionic acid ethyl esterHCID 5439709971.2%

Reaction Steps

A solution of 3-cyclopentyl-2-(4-ethanesulfonyl-phenyl)-acrylic acid ethyl ester [4.89 g, 14.53 mmol, (E):(Z)=3:1] in ethanol (36 mL) was slowly treated with 10% palladium on activated carbon (244.5 mg). The reaction mixture was stirred under a positive pressure of hydrogen gas (balloon) at 25° C. and atmospheric pressure for 44 h. The catalyst was then filtered off through a pad of celite, and the celite pad was washed well with ethyl acetate. The filtrate was concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 3/1 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-ethanesulfonyl-phenyl)-propionic acid ethyl ester (3.50 g, 71%) as a colorless viscous oil: FAB-LRMS m/e calcd for C18H26O4S (M+H)+ integer mass 338, found 339.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-6bb930f89c5643d68de87a98bca1b353
Source noteuspto-grants-2003_08