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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081228Generated: October 27, 2026

Benzoyl chloride → 2-Phenyl-1,3-benzoxazol-6-ol

https://huagongshe.com/reaction/1081228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant4-Aminobenzene-1,3-diol hydrochlorideHCID 13408822—
Product2-Phenyl-1,3-benzoxazol-6-olHCID 835869—

Reaction Steps

0.005 mol of 4-aminoresorcinol hydrochloride were dissolved in 7.5 ml of benzoyl chloride, while heating, and the solution was then boiled under reflux for 7 hours. The excess benzoyl chloride was subsequently distilled off in vacuo, 10 ml of ethanol were added to the residue and the mixture was boiled up briefly and, after cooling, rendered alkaline with 10 M NaOH solution. The alkaline solution was introduced into 200 ml of water and brought to pH 3 with concentrated hydrochloric acid, using a pH-meter. The crystal mass which precipitated here was filtered off with suction and recrystallized from 15 ml of toluene. The dried product (250 mg) was uniform according to thin layer chromatography (silica gel plate, ethyl acetate/glacial acetic acid 24:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05585247
Source datasetuspto-grants-1996_12
ORD IDord-a9ee15ea29584ca28fe4851de2657377
Source noteuspto-grants-1996_12