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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884722Generated: October 30, 2026

Pyridine → HCID 135427889, compound

https://huagongshe.com/reaction/884722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSalicylamideHCID 5147—
Reactantp-Acetoxybenzoyl chlorideHCID 2756254—
SolventO-XyleneHCID 7237—
ProductHCID 135427889HCID 13542788912%

Reaction Steps

Salicylamide (6.85 g, 50 mmol) and 4-acetoxybenzoyl chloride (10.9 g, 55 mmol) were dissolved in 35 mL anhydrous xylene. Anhydrous pyridine (0.5 mL) was added and the reaction mixture was refluxed under nitrogen for 12 h. Water was removed by a Dean-Stark apparatus. The mixture was cooled to rt, and the xylene was removed under vacuum. Acetone (100 mL) was added and the mixture was stirred for 10 min. The solid was filtered off, washed with acetone and dried under vacuum to give the crude compound (3.0 g). The crude compound (1.5 g) was purified by column chromatography (SilicaGel 70-230 mesh; 2-5% MeOH in DCM as eluent) to give 770 mg of 2-(4-hydroxyphenyl)benzo[e][1,3]oxazin-4-one (12%) as pale yellow solid. MS (ES) m/z: 240.02; Mp. 273-275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242130B2
Source datasetuspto-grants-2012_08
ORD IDord-2ad357a5885f49daae66ed7afc063ac6
Source noteuspto-grants-2012_08