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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270316Generated: November 2, 2026

Methyl iodide → 2-(4-Methoxy-benzenesulfonyl)-2-methyl-3-phenyl-propionic acid ethyl ester

https://huagongshe.com/reaction/2270316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant2-(4-Methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl esterHCID 10893429—
SolventAcetoneHCID 180—
Product2-(4-Methoxy-benzenesulfonyl)-2-methyl-3-phenyl-propionic acid ethyl esterHCID 10948439—

Reaction Steps

To a stirred solution of 2-(4-methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl ester (1.0 gm, 3mmol) (example 9), methyl iodide (1 ml, excess) and 18-Crown-6 (500 mg) in acetone (250 ml), K2CO3 (10 gm, excess) was added and the reaction mixture was refluxed for 24 hours. At the end, the reaction mixture was filtered and the acetone layer was concentrated. The residue obtained was extracted with chloroform, washed well with water, dried over anhydrous MgSO4, filtered and concentrated. The product obtained was purified by silica-gel column chromatography by eluting it with 30% ethyl acetate:hexanes to afford 2-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-propionic acid ethyl ester as a colorless oil. Yield 1.0 g, 98%; MS: 349 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331563B1
Source datasetuspto-grants-2001_12
ORD IDord-cf72853bd6e343879bb30e40919c66e6
Source noteuspto-grants-2001_12