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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370409Generated: October 30, 2026

Triethylamine → n-[2-[2-(1,1-Dimethyl-2-propenyl)-1h-indol-3-yl]ethyl]-carbamic acid phenylmethyl ester

https://huagongshe.com/reaction/1370409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant2-(1,1-dimethyl-2-propenyl)-1H-indole-3-ethanamineHCID 22396740—
SolventDichloromethaneHCID 6344—
Productn-[2-[2-(1,1-Dimethyl-2-propenyl)-1h-indol-3-yl]ethyl]-carbamic acid phenylmethyl esterHCID 69792966—

Reaction Steps

To a solution of 2-(1,1-dimethyl-2-propenyl)-1H-indole-3-ethanamine (0.707 g, 3.07 mmol) in dry CH2Cl2 (30 mL) at 0° C. under argon was added NEt3 (0.98 mL, 6.93 mmol) and BnOC(O)Cl (1.10 mL, 7.32 mmol). The reaction was permitted to warm to rt while stirring overnight. It was diluted with CH2Cl2, and extracted with cold H2O. The CH2Cl2 layer was separated. The H2O layer was re-extracted with CH2Cl2. The combined CH2Cl2 extracts were washed with satd aq NaHCO3 and brine, dried, filtered and concentrated to give an oil. This oil was purified by silica chromatography to provide the title compound: TLC Rf=0.34 (CH2Cl2); MS (EI) m/z 362.3, 254, 211, 198, 182. 168, 167, 108, 91, 77, 65, 51; 1H NMR (300 MHz, CDCl3) δ 7.89 (1H), 7.56 (1H), 7.33-7.26 (6H), 7.10 (2H), 6.12 (1H), 5.18-5.12 (2H), 5.12 (2H), 4.87 (1H), 3.47 (2H), 3.07 (2H), 1.53 (6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583135B2
Source datasetuspto-grants-2003_06
ORD IDord-9e5f6684aa474e13a766aaebd54436ca
Source noteuspto-grants-2003_06