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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30554Generated: October 25, 2026

Benzoyl chloride, 3-bromo- → 3-Bromo-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/30554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-bromo-HCID 74377—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
Product3-Bromo-N-methoxy-N-methylbenzamideHCID 1216287590.3%

Reaction Steps

A mixture of N-methoxymethanamine hydrochloride (22.1 g, 228.5 mmol), diisopropyl ethyl amine (63.5 mL, 365.6 mmol) and CH2Cl2 was treated dropwise with 3-bromobenzoyl chloride (15 g, 68.5 mmol) in CH2Cl2, stirred at room temperature for 30 minutes, and concentrated under vacuum. The resultant residue was dispersed in water and extracted with ethyl ether. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. The resultant residue was purified on silica gel (Biotage) using hexanes/EtOAc (2/1) as the eluting solvents to give 3-bromo-N-methoxy-N-methylbenzamide as a tan solid (15.1 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423158B2
Source datasetuspto-grants-2008_09
ORD IDord-166da1d9e33a4bd8acda9bd0700ddbfe
Source noteuspto-grants-2008_09