Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219694Generated: October 29, 2026

Phosphorus oxychloride → 2-tert-Butyl-4-chloro-6-cyclopropyl-pyrimidine

https://huagongshe.com/reaction/219694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178441865HCID 178441865—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product2-tert-Butyl-4-chloro-6-cyclopropyl-pyrimidineHCID 63355304104.9%

Reaction Steps

14.8 g 2-tert-butyl-4-hydroxy-6-cyclopropyl-pyrimidine (76.9 mmol) were dissolved in 100 ml of toluene and 3 ml of dimethylformamide. 23.6 ml of POCl3 (153.7 mmol) were added dropwise at 10° C. After stirring overnight at room temperature most of the toluene was evaporated. The mixture was cooled with ice and 20 ml of water were added cautiously. Subsequently, an additional 200 ml of water were added and the aqueous phase was extracted four times with dichloromethane. The combined organic phases were dried over magnesium sulfate, filtered, and then concentrated to dryness to yield 17 g of a yellowish oil (quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202868B2
Source datasetuspto-grants-2012_06
ORD IDord-8f760cff3ce9466ea5589371ac324223
Source noteuspto-grants-2012_06