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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467995Generated: October 31, 2026

Triethylamine → ethyl 1H-indol-5-ylcarbamate

https://huagongshe.com/reaction/1467995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant5-AminoindoleHCID 78867—
SolventDichloromethaneHCID 6344—
Productethyl 1H-indol-5-ylcarbamateHCID 5403388535.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 1H-indol-5-amine (11 g, 83.2 mmol) and triethyl amine (25.22 g, 250 mmol) in dichloromethane (110 mL) at −10° C., ethyl-chloro-formate (13.5 g 124.8 mmol) was added dropwise and stirred at 0° C. for 2-3 h. The reaction was quenched with water and the mixture was extracted with ethyl acetate. The organic layer was concentrated in vacuo and the resultant residue was purified by flash column chromatography to give ethyl-1H-indol-5-ylcarbamate (5.980 g, 35.2%); MS: 205 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000175B2
Source datasetuspto-grants-2015_04
ORD IDord-7af1d86742654a98bab712e45762843f
Source noteuspto-grants-2015_04