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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264396Generated: October 26, 2026

Water → (RS)-2-(2-buten-1-yl)-6-bromo-1-indanone

https://huagongshe.com/reaction/264396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-Buten-2-olHCID 11716—
Reactant1-Indanone, 6-bromo-HCID 139778—
Solvent2,2-DimethoxypropaneHCID 6495—
Product(RS)-2-(2-buten-1-yl)-6-bromo-1-indanoneHCID 5368740178%

Reaction Steps

A solution of 10.0 g of 6-bromo-1-indanone, 9.79 ml of 3-buten-2-ol and 100 mg of p-toluenesulfonic acid in 100 ml of 2,2-dimethoxypropane was boiled under reflux for 71 hours on a water separator filled with molecular sieve (0.4 nm, 2 mm pearl shaped). The reaction mixture was subsequently concentrated in a vacuum and purified by column chromatography on silica gel (hexane/diethyl ether 1:1). In addition to 3.07 g of educt, there were obtained 9.86 g (78%) of (RS)-2-(2-buten-1-yl)-6-bromo-1-indanone as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-48bf84bd6a0d4d789dc293b7da95298b
Source noteuspto-grants-1997_07