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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305843Generated: October 27, 2026

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

https://huagongshe.com/reaction/2305843

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 chromatography, eluting with 30% ethy acetate: hexane. The product 2-(4methoxy-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 numberUS06441023B1
Source datasetuspto-grants-2002_08
ORD IDord-9b258b5987fc433b8203320c5271512a
Source noteuspto-grants-2002_08