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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918544Generated: October 31, 2026

Phenyl chloroformate → phenyl 2-(5-chloro-1H-indol-3-yl)ethylcarbamate

https://huagongshe.com/reaction/1918544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
SolventDichloromethaneHCID 6344—
Productphenyl 2-(5-chloro-1H-indol-3-yl)ethylcarbamateHCID 6683188288.2%

Reaction Steps

N,N-diisopropylethylamine (0.745; 4.33 mmol) was added to a mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.500 g; 2.16 mmol), and phenyl chloroformate (0.406 mL; 3.25 mmol) in dichloromethane (20 mL). The solution was stirred at room temperature. for 20 minutes, diluted in dichloromethane, washed with sodium hydrogen sulfate (1M, water), sodium carbonate (1M, water) and brine. The organic layer was dried and concentrated under reduced pressure to furnish 0.60 g (88%) of phenyl 2-(5-chloro-1H-indol-3-yl)ethylcarbamate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-55121b087d9f42be8fa2a32a3897773d
Source noteuspto-grants-2013_12