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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264452Generated: October 29, 2026

Water → (S)-1-(7-chloro-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol

https://huagongshe.com/reaction/264452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(S)-(+)-1-Aminopropan-2-olHCID 7311736—
Reactant(RS)-2-(2-oxoethyl)-6-chloro-1-indanoneHCID 10608460—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product(S)-1-(7-chloro-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-olHCID 1068196953%

Reaction Steps

A solution of 2.5 g of (RS)-2-(2-oxoethyl)-6-chloro-1-indanone and 100 mg of p-toluenesulfonic acid in 120 ml in anhydrous toluene was heated on a water separator. A solution of 3.6 g of (S)-1-amino-2-propanol in 20 ml of anhydrous toluene was added dropwise to the boiling solution over a period of 5 minutes. Subsequently, the mixture was boiled for 30 minutes, during which the solvent was reduced to a volume of 20 ml. The cooled reaction mixture was purified by column chromatography on silica gel (ethyl acetate/toluene 1:1). 1.56 g (53%) of (S)-1-(7-chloro-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol were obtained as a brown oil which was used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-57fc7dfea757400295a83745f69d79ba
Source noteuspto-grants-1997_07