Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114688Generated: October 30, 2026

Oxalyl chloride → 2-(4-Bromophenyl)-N-{2-(3-methoxyphenyl)ethyl}-N-phenylacetamide

https://huagongshe.com/reaction/2114688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantBenzeneacetyl chloride, 4-bromo-HCID 181552—
ReactantBromophenylacetyl chlorideHCID 598182—
ReactantHCID 13467414HCID 13467414—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-(4-Bromophenyl)-N-{2-(3-methoxyphenyl)ethyl}-N-phenylacetamideHCID 2344079898%

Reaction Steps

To a solution of {2-(3-methoxyphenyl)ethyl}phenylamine (1.06 g, 4.65 mmol) in ethyl acetate (80 mL) under nitrogen was added a solution of 4-bromophenylacetyl chloride (1.06 g, 4.65 mmol) in ethyl acetate (20 mL), the bromophenylacetyl chloride being prepared from the corresponding carboxylic acid (1 g, 4.65 mmol) and oxalyl chloride (0.61 mL, 6.98 mmol) in CH2Cl2 (20 mL). After 1 hour, the reaction was poured into water (50 mL). The organic layer was dried over MgSO4, filtered and concentrated to provide the title compound (1.92 g, 98% yield): EI-MS (m/z) 423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435729B2
Source datasetuspto-grants-2008_10
ORD IDord-9b08ec991c374ad9b81ec4e3b058431f
Source noteuspto-grants-2008_10