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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515161Generated: October 30, 2026

Triethylamine → HCID 86699733, compound

https://huagongshe.com/reaction/515161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-ChlorobenzylamineHCID 66036—
Reactant4-Bromo-2-methoxy-6-methylbenzoic acidHCID 45480386—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 86699733HCID 8669973392.6%

Reaction Steps

To a stirred solution of 4-bromo-2-methoxy-6-methyl-benzoic acid (1.2 g, 4.89 mmol) in dichloromethane (10 ml) are added oxalyl chloride (0.52 ml, 5.86 mmol) and dimethylformamide (catalytic amount) at 0° C. The reaction mixture is stirred for 30 min at RT. Excess oxalyl chloride is distilled off under nitrogen. The residue is dissolved in dichloromethane (10 ml), cooled to 0° C. followed by the addition of triethylamine (1.7 ml, 12.2 mmol) and 4-chlorobenzylamine (0.71 ml, 5.86 mmol). The reaction mixture is stirred for 1 h at RT. After completion of the reaction (monitored by TLC) the mixture is diluted with water (50 ml) and extracted with dichloromethane (3×50 ml). The organic layer is washed with water (50 ml), brine (50 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 15% ethyl acetate/hexane) to yield 4-bromo-N-[(4-chlorophenyl)-methyl]-2-methoxy-6-methyl-benzamide (1.67 g, 4.53 mmol, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-06229f009a084581b103b4a36615020c
Source noteuspto-grants-2015_08