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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584840Generated: October 25, 2026

Oxalyl chloride → 2-Chloro-4-methylpyrimidine-5-carbonyl chloride

https://huagongshe.com/reaction/1584840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Chloro-4-methylpyrimidine-5-carboxylic acidHCID 10487414—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-methylpyrimidine-5-carbonyl chlorideHCID 2122065061.3%

Reaction Steps

A solution of 2-chloro-4-methylpyrimidine-5-carboxylic acid (0.81 g, 4.70 mmol), oxalyl chloride (0.89 g, 7.05 mmol), DMF (2 drops) in CH2Cl2 (23 mL) was stirred at room temperature under N2 for 4 h. The solution was concentrated and distilled to give the title compound (0.55 g, 61%); b.p. 90-100° C., 1.3 mm/Hg; 1H NMR (CDCl3) δ d9.02 (s, 1H), 2.74 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935966
Source datasetuspto-grants-1999_08
ORD IDord-d375475290144e0fa6610171f81d8166
Source noteuspto-grants-1999_08