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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394274Generated: November 2, 2026

Oxalyl chloride → 2-Cyano-4-(trifluoromethyl)-5-pyrimidinecarbonyl chloride

https://huagongshe.com/reaction/2394274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Cyano-4-trifluoromethylpyrimidine-5-carboxylic acidHCID 10584856—
CatalystDimethylformamideHCID 6228—
SolventChlorineHCID 24526—
Product2-Cyano-4-(trifluoromethyl)-5-pyrimidinecarbonyl chlorideHCID 1079976983.1%

Reaction Steps

A solution of 2-cyano-4-trifluoromethylpyrimidine-5-carboxylic acid (2.0 g, 9.2 mmol), oxalyl chloride (1.4 g, 11 mmol) and DMF (4 drops) in CH2 Cl2 (46 mL) was stirred at room temperature under N2 for 0.75 h. The reaction was concentrated and distilled (b.p. 100° C., 1.5 mm/Hg) to give the title compound (1.8 g, 82% yield); 1HNMR (CDCl3) δ 9.49 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811428
Source datasetuspto-grants-1998_09
ORD IDord-dd830d0144254084ac1e1e3106c68e28
Source noteuspto-grants-1998_09