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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027209Generated: October 29, 2026

Triethylamine → 3-(benzyloxy)-4-bromo-5-methoxy-N-(prop-2-yn-1-yl)benzamide

https://huagongshe.com/reaction/1027209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantPropargylamineHCID 239041—
Reactant3-(Benzyloxy)-4-bromo-5-methoxybenzoic acidHCID 86710605—
CatalystDimethylformamideHCID 6228—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product3-(benzyloxy)-4-bromo-5-methoxy-N-(prop-2-yn-1-yl)benzamideHCID 8671060684.7%

Reaction Steps

To a suspension of 3-(benzyloxy)-4-bromo-5-methoxybenzoic acid (2.0 g, 5.93 mmol) and 4 drops of DMF in DCM (40 mL) was slowly added oxalyl chloride (0.57 mL, 6.52 mmol). After three hours the solvent was removed and the residue redissolved into DCM (10 mL). To this solution was slowly added a mixture of propargylamine (0.46 mL, 7.12 mmol) and triethylamine (2.5 mL, 17.8 mmol) in DCM (2 mL). After 30 minutes the solution was diluted with ether, washed with water (2×), 1 M hydrochloric acid (2×), water, saturated sodium bicarbonate, brine, dried over magnesium sulfate and concentrated to a yellow solid. The solid was triturated with diethyl ether and dried under vacuum to provide 3-(benzyloxy)-4-bromo-5-methoxy-N-(prop-2-yn-1-yl)benzamide (1.88 g) as an off-white solid. MS=374.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-f7c152ec1bad4ba89709a6e156946b4b
Source noteuspto-grants-2014_05