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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264431Generated: November 1, 2026

1-Amino-2-propanol → (RS)-1-(7-chloro-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol

https://huagongshe.com/reaction/264431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Amino-2-propanolHCID 4—
ReactantWaterHCID 962—
Reactant(RS)-2-(2-oxoethyl)-6-chloro-1-indanoneHCID 10608460—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product(RS)-1-(7-chloro-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-olHCID 1903640661.5%

Reaction Steps

A solution of 2.08 g of (RS)-2-(2-oxoethyl)-6-chloro-1-indanone and 80 mg of p-toluenesulfonic acid in 70 ml of anhydrous toluene was heated on a water separator. A solution of 3.0 g of (RS)-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 an additional 45 minutes, during which the solvent was reduced to a volume of 30 ml. The cooled reaction mixture was purified by column chromatography on silica gel (ethyl acetate/toluene 3:7). 1.52 g (61%) of (RS)-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-aabf89dca7a44a2eb238f2270bda1b3c
Source noteuspto-grants-1997_07