Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251325Generated: November 1, 2026

Phosphorus oxychloride → 4-Chloro-6-(trifluoromethyl)quinazoline

https://huagongshe.com/reaction/251325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178517998HCID 178517998—
Product4-Chloro-6-(trifluoromethyl)quinazolineHCID 21075095—

Reaction Steps

A suspension of 6-(trifluoromethyl)quinazolin-4-ol (10.41 g, 48.4 mmol) in phosphorous oxychloride (100 mL) was heated at reflux for 3 h, during which time a clear, amber solution was observed. The solution was cooled to room temperature, concentrated in-vacuo, and stripped 3× from 150 mL methylene chloride to remove any remaining phosphorous oxychloride. The residue was partitioned between EtOAc and saturated sodium bicarbonate (1:1, 300 mL), and the mixture was stirred until gas evolution ceased. The layers were separated, the organic phase was washed successively with saturated sodium bicarbonate and brine, the combined aqueous phases were extracted with EtOAc (50 mL), and the combined organic phases were dried over sodium sulfate then concentrated in-vacuo. The residue was purified over silica gel, eluting with 25% EtOAc/Heptane, to yield 8.14 g of 4-chloro-6-(trifluoromethyl)quinazoline as a white solid. MS (ES+)=233, 235 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863333B2
Source datasetuspto-grants-2011_01
ORD IDord-75548fe590de4d51beaadd2ff26eee03
Source noteuspto-grants-2011_01