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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251385Generated: October 25, 2026

Potassium Carbonate → 2-(4-Methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester

https://huagongshe.com/reaction/1251385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
ReactantBromoisopreneHCID 53976308—
SolventAcetoneHCID 180—
Product2-(4-Methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl esterHCID 11759197—

Reaction Steps

To a stirred solution of (4-methoxy-benzenesulfonyl)-acetic acid ethyl ester (5.16 g, 20 mmol), isoprenyl bromide (3.0 g, 20 mmol) and 18-Crown-6 (500 mg) in acetone (250 ml) was added K2CO3 (10 gms, excess) and the mixture refluxed foe 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 chromoatography, eluting with 30% ethyl acetate:hexane. The product 2-(4-methoxy-benzenesulfonyl)-5-methyl-hex-4-enoic acid ethyl ester was isolated as a colourless oil. Yield: 3.0 g, 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342508B1
Source datasetuspto-grants-2002_01
ORD IDord-6a87bd2a2d014c099254d3f240196918
Source noteuspto-grants-2002_01