Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253611Generated: November 4, 2026

Dimethylformamide → 5-Bromopyrimidine-2-carbonyl chloride

https://huagongshe.com/reaction/1253611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Bromopyrimidine-2-carboxylic acidHCID 16462970—
CatalystDimethylformamideHCID 6228—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product5-Bromopyrimidine-2-carbonyl chlorideHCID 59674657100%

Reaction Steps

Oxalyl chloride (47.4 g, 369 mmol) was added to a suspension of 5-Bromo-pyrimidine-2-carboxylic acid (50 g, 250 mmol) in dichloromethane (821 ml) at room temperature followed by 1-2 drop of dimethylformamide. The reaction mixture was stirred under nitrogen for 2 hours LCMS in methanol indicated the presence of the methyl ester and some acid. Dimethylformamide (0.2 ml) was added to the reaction mixture. The acid dissolved after 30 minutes. LCMS showed corresponding methyl ester and no starting material peak was observed. The solvent was removed and dried in vacuo to afford the crude 5-Bromo-pyrimidine-2-carbonyl chloride (55 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455496B2
Source datasetuspto-grants-2013_06
ORD IDord-ce341de1623a48fea811032cf123be48
Source noteuspto-grants-2013_06