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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264514Generated: November 1, 2026

Water → (RS)-2-(2-buten-1-yl)-5,6-dichloro-1-indanone

https://huagongshe.com/reaction/264514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-Buten-2-olHCID 11716—
Reactant5,6-Dichloro-2,3-dihydro-1H-inden-1-oneHCID 22903609—
Solvent2,2-DimethoxypropaneHCID 6495—
Product(RS)-2-(2-buten-1-yl)-5,6-dichloro-1-indanoneHCID 5396094769%

Reaction Steps

A solution of 12.3 g of 5,6-dichloro-1-indanone, 12.6 ml of 3-buten-2-ol and 125 mg of p-toluenesulfonic acid in 125 ml of 2,2-dimethoxy-propane was boiled under reflux for 68 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 4:1). In addition to 4.3 g of educt, there were obtained 10.8 g (69%) of (RS)-2-(2-buten-1-yl)-5,6-dichloro-1-indanone as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-427881176dcb4f238913865a6a187e5f
Source noteuspto-grants-1997_07