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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226942Generated: October 26, 2026

Triethylamine → N-ethoxycarbonyl-m-bromophenethylamine

https://huagongshe.com/reaction/2226942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant3-BromophenethylamineHCID 7021736—
SolventDichloromethaneHCID 6344—
ProductN-ethoxycarbonyl-m-bromophenethylamineHCID 18963948—

Reaction Steps

A solution of m-bromophenethylamine (6.71 g, 33.55 mmol) and Et3N (7 mL, 50.32 mmoL) in CH2Cl2 (100 mL) is cooled to 0° and ethyl chloroformate (4 mL, 50.32 mmoL) is added. After addition is complete the resulting mixture is allowed to come to room temperature and the solvent is removed in vacuo. The residue is then dissolved in EtOAc (200 mL) and the organic phase washed with 2N HCl (1×250 mL), H2O (1×200 mL), saturated NaHCO3 solution (1×200 mL), saturated NaCl solution (1×200 mL), dried over MgSO4 and concentrated in vacuo to give N-ethoxycarbonyl-m-bromophenethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350761
Source datasetuspto-grants-1994_09
ORD IDord-c63629e8fdbf48d994aba8e9dcf2a662
Source noteuspto-grants-1994_09