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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185907Generated: October 30, 2026

Triethylamine → 3-(3,4-Difluorophenyl)4-(ethoxycarbonylamino)-1-butanol

https://huagongshe.com/reaction/2185907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant4-Amino-3-(3,4-difluorophenyl)-1-butanolHCID 22452637—
SolventDichloromethaneHCID 6344—
Product3-(3,4-Difluorophenyl)4-(ethoxycarbonylamino)-1-butanolHCID 2245267788%

Reaction Steps

Ethyl chloroformate (3.9 mL, 40.8 mmol) was added dropwise to a stirred cooled (−40° C.) solution of 4-amino-3-(3,4-difluorophenyl)-1-butanol (7.45 g, 37 mmol) and triethylamine (5.94 mL, 42.6 mmol) in DCM (180 mL). The solution was stirred at room temperature for 30 min and at room temperature overnight. The material was washed twice with 1N HCl, twice with saturated sodium bicarbonate; dried (Na2SO4), filtered and the solvent removed to provide the title compound (8.85 g, 88%) as a yellow oil. 1H-NMR (CDCl3) δ 1.18-1.23 (t, 3H, CH) 1.72-1.98 (m, 3H) 2.96-3.00 (m, 1H, CH) 3.24-3.29 (m, 1H, CH) 3.45-4.04 (m, 3H, CH), 4.06-4.14 (m, 2H, CH) 4.66 (br. s, 1H, OH or NH) 6.91-7.37 (m, 3H, ArH). MS m/z 274 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403601B1
Source datasetuspto-grants-2002_06
ORD IDord-9f2baada93884e98bedf46a8e507599e
Source noteuspto-grants-2002_06