Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283263Generated: October 26, 2026

Phosphorus pentachloride → 2-[2-(5-Nitro-2-furyl)vinyl]-4-chloroquinazoline

https://huagongshe.com/reaction/1283263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus pentachlorideHCID 24819—
Reactant2-[2-(5-nitro-2-furyl)vinyl]-4-(3H)quinazolinoneHCID 136114329—
SolventPhosphorus oxychlorideHCID 24813—
Product2-[2-(5-Nitro-2-furyl)vinyl]-4-chloroquinazolineHCID 5363407967%

Reaction Steps

A 500 ml 3 necked flash fitted with a stirrer, reflux condenser and protected by a calcium chloride trap was charged with 9.0 g of phosphorus pentachloride (0.043 mole) and 70 ml of phosphorus oxychloride and the mixture stirred. To this 11.3 g (0.04 mole) of 2-[2-(5-nitro-2-furyl)vinyl] -4-(3H)quinazolinone was added and rinsed into the flask with 15 ml of phosphorus oxychloride. The mixture was heated under reflux for 4 hours, cooled in an ice bath and diluted with 150 ml of diethyl ether. The 2-[2-(5-nitro-2-furyl)vinyl]-4-chloroquinazoline which precipitated was collected by filtration, washed with 100-150 ml of diethyl ether, slurried in 100 ml of diethyl ether and then refiltered to obtain 8.09 g of the desired product melting at 252°-4°C with decomposition. The product was recrystallized from toluene (large volumes are required) or was extracted in a Soxhlet extractor with toluene to obtain yellow crystals of 2-[2-(5-nitro-2-furyl)vinyl]-4-chloroquinazoline melting at 264°-5°C with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03974277
Source datasetuspto-grants-1976_08
ORD IDord-ef27a5aea8c6427785069fb05d9e0e84
Source noteuspto-grants-1976_08