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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40275Generated: October 26, 2026

Diisopropylethylamine → 4-bromo-2-chloro-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/40275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-2-chlorobenzoic acidHCID 108829—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
Product4-bromo-2-chloro-N-methoxy-N-methylbenzamideHCID 59843076—

Reaction Steps

To a stirring solution of 4-bromo-2-chlorobenzoic acid (3.45 g, 15 mmol) and DIEA (7.7 ml, 44 mmol) in DMF (30 mL) was added HATU (6.1 g, 16 mmol) at 23° C. under nitrogen. Darkened suspension stirred for 1 h, then added n,o-dimethylhydroxylamine hydrochloride (2.1 g, 22 mmol). Solution stirred overnight at 23° C. Reaction then partitioned between 2.5% NaHCO3 (250 mL) and diethyl ether (100 mL). Aqueous further extracted with ether (2×50 mL). Combined ethereal extracts dried over MgSO4, then concentrated an amber oil under reduced pressure. 4-bromo-2-chloro-N-methoxy-N-methylbenzamide isolated as a light amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524900B2
Source datasetuspto-grants-2013_09
ORD IDord-d5ed4a33c06849c1a8e5bfa29170ba08
Source noteuspto-grants-2013_09