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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946663Generated: October 27, 2026

Phosphorus oxychloride → 6-Chloropyrimidine-4-carbonyl chloride

https://huagongshe.com/reaction/1946663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178524636HCID 178524636—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product6-Chloropyrimidine-4-carbonyl chlorideHCID 18422098—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred mixture of 6-hydroxypyrimidine-4-carboxylic acid (10.0 g, 71.4 mmol, prepared according to the method described by Daves, G. C.; Baiocchi, F.; Robins, R. K.; Cheng, C. C. in J. Org. Chem. 1961, 26, 2755-2763) and phosphorus pentachloride (58.0 g, 0.27 mol) was treated with phosphorus oxychloride (100 mL, 1.07 mol) and the resultant mixture was refluxed for 16 hours under nitrogen. The excess phosphorus oxychloride was distilled off and the residue was azeotroped three times with toluene and dried in vacuo. The solid product obtained was suspended in dry dichloromethane (100 mL), cooled (0° C.) and treated with dry DMF (2 mL) and oxalyl chloride (7.9 mL, 91 mmol). The resultant mixture was stirred at room temperature for 15 hours and evaporated in vacuo to afford 6-chloropyrimidine-4carbonyl chloride as a brown liquid, which was used for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-c5cbdabdf2264bed9a6b5f84ca607ddc
Source noteuspto-grants-2013_03