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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50618Generated: November 1, 2026

Triethylamine → N-isopropyl-6-phenoxycarbonylamino-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/reaction/50618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
ReactantN-isopropyl-6-amino-1,2,3,4-tetrahydrocarbazoleHCID 12992579—
SolventDichloromethaneHCID 6344—
ProductN-isopropyl-6-phenoxycarbonylamino-1,2,3,4-tetrahydrocarbazoleHCID 2273614715.1%

Reaction Steps

The N-isopropyl-6-amino-1,2,3,4-tetrahydrocarbazole (9.84 g) and 5.05 g of triethylamine were dissolved in 100 mL of dichloromethane, and added dropwise with 7.85 g of phenyl chloroformate. The reaction mixture was stirred at room temperature for 3 hours, then washed with 10% aqueous citric acid and then with saturated aqueous sodium hydrogencarbonate, and dried over anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel chromatography (eluent: hexane/ethyl acetate=8/2) and recrystallized from a mixture of hexane and ethyl acetate, to obtain 2.27 g of N-isopropyl-6-phenoxycarbonylamino-1,2,3,4-tetrahydrocarbazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713473B1
Source datasetuspto-grants-2004_03
ORD IDord-38f8ccac7ecc46768baf854bdb1c427c
Source noteuspto-grants-2004_03