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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247890Generated: October 25, 2026

2-Chlorobenzoyl chloride → 2-(2-chlorophenyl)-3-hydroxy-4(3H)-quinazolinone

https://huagongshe.com/reaction/1247890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl chlorideHCID 69110—
Reactant2-Aminobenzohydroxamic acidHCID 79721—
Solvent1,4-DioxaneHCID 31275—
Product2-(2-chlorophenyl)-3-hydroxy-4(3H)-quinazolinoneHCID 148733952%

Reaction Steps

35 g (0.2 mol) of o-chlorobenzoyl chloride are added to a solution of 30.4 g (0.2 mol) of o-aminobenzhydroxamic acid in 250 ml of dioxane at 20°-30° C. The mixture is boiled under reflux for 3 hours, the solvent is then distilled in vacuo, 100 ml of ether are added to the residue, and the crystalline product is filtered off under suction. It is dissolved in 300 ml of 5% strength sodium hydroxide solution, the solution is filtered and the filtrate is acidified with concentrated hydrochloric acid. The precipitated product is then filtered off under suction and rinsed with water. In this manner, 28.2 g (52% of theory) of 2-(2-chlorophenyl)-3-hydroxy-3,4-dihydro-4-oxo-quinazoline are obtained in the form of crystals of melting point 211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04521420
Source datasetuspto-grants-1985_06
ORD IDord-03f47d74676c47f6acf5e539125591e5
Source noteuspto-grants-1985_06