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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221316Generated: November 2, 2026

Diisopropylethylamine → benzyl (2S)-1-[(2R)-2-bromopropionyl]-2,3,4,5,6,7-hexahydro-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2221316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(2R)-2-bromopropionyl chlorideHCID 6997261—
ReactantBenzyl (2S)-2,3,4,5,6,7-hexahydro-1H-indole-2-carboxylateHCID 11253898—
SolventDichloromethaneHCID 6344—
Productbenzyl (2S)-1-[(2R)-2-bromopropionyl]-2,3,4,5,6,7-hexahydro-1H-indole-2-carboxylateHCID 11440745—

Reaction Steps

Introduce 200 g of benzyl (2S)-2,3,4,5,6,7-hexahydro-1H-indole-2-carboxylate and 1.5 litres of dichloromethane into a reactor, then bring the temperature of the reaction mixture to 0° C. and add 201 ml of diisopropylethylamine followed by 132 g of (2R)-2-bromopropionyl chloride. Subsequently, bring the mixture to ambient temperature. After stirring for 1 hour at that temperature, wash the mixture with water and then with a dilute acetic acid solution. The benzyl (2S)-1-[(2R)-2-bromopropionyl]-2,3,4,5,6,7-hexahydro-1H-indole-2-carboxylate solution so obtained is used as it is in the following Step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368580B2
Source datasetuspto-grants-2008_05
ORD IDord-66c85d7a3390450ba8e6fad5085e1c86
Source noteuspto-grants-2008_05