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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055530Generated: November 1, 2026

Triethylamine → 1-(5-Bromo-2-chlorophenyl)-2-[methoxy(methyl)amino]ethanone

https://huagongshe.com/reaction/1055530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
SolventDichloromethaneHCID 6344—
Product1-(5-Bromo-2-chlorophenyl)-2-[methoxy(methyl)amino]ethanoneHCID 118377792100%

Reaction Steps

To a solution of N,O-dimethyl hydroxylamine hydrochloride (1.0 g, 10.25 mmol) in dichloromethane (50 mL) was added triethyl amine (3.10 g, 30.75 mmol). The mixture was stirred at room temperature for 10 min followed by adding 5-bromo-2-chloro-benzoic acid 15a (2.41 g, 10.25 mmol, purchased from Beijing yu xiang hui da chemical co., LTD) and bis(2-oxo-3-oxazolidiny)phosphonic chloride (3.13 g, 12.3 mmol) in turn. The resulting mixture was further stirred for 23 hours. The reaction mixture was quenched with 40 mL of water and extracted with ethyl acetate (40 mL×3). The combined organic layers were washed with saturated brine (50 mL×3), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to give the title compound 15b as a white solid (2.90 g, 100%). The crude product was used in next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394329B2
Source datasetuspto-grants-2016_07
ORD IDord-a3b12eafba6948ee80da2ad1ce292c45
Source noteuspto-grants-2016_07