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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281302Generated: November 1, 2026

Diethylamine → HCID 44253972, compound

https://huagongshe.com/reaction/2281302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-Bromo-2-methylbenzoic acidHCID 99570—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 44253972HCID 44253972—

Reaction Steps

A solution of 4-bromo-2-methylbenzoic acid (25 g, 120 mmol) in DCM (400 mL) was treated with oxalyl chloride (12 mL, 130 mmol) and a catalytic amount of dry DMF (0.10 mL). The reaction was allowed to stir under nitrogen for 2 hours at room temperature. Removal of excess solvent gave crude acid chloride which was re-dissolved in DCM (400 mL). The mixture was then cooled to 0° C. and triethylamine (41 mL, 290 mmol) was added followed by the slow addition of diethyl amine (24 mL, 233 mmol). The reaction was then allowed to warm to room temperature overnight. The crude mixture was then diluted with 400 mL of water and extracted with DCM (3×500 mL). The combined organic layers were then washed with brine (200 mL), dried over magnesium sulfate, filtered and then concentrated. The crude material was purified via MPLC (10% EtOAc/Hex) to afford 4-bromo-N,N-diethyl-2-methylbenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139585B2
Source datasetuspto-grants-2015_09
ORD IDord-39e75a15f55b4924af6b1d44441823e2
Source noteuspto-grants-2015_09