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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585443Generated: October 30, 2026

Phenacyl bromide → 7-methyl-3-phenyl-2H-1,4-benzoxazine

https://huagongshe.com/reaction/585443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-5-methylphenolHCID 76082—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product7-methyl-3-phenyl-2H-1,4-benzoxazineHCID 1091116949.4%

Reaction Steps

To potassium carbonate (63.89 g, 462 mmol) in water (300 mL) and CH2Cl2 (200 mL) is added 6-amino-m-cresol (10.0 g, 81.2 mmol) and tetra-n-butyl ammonium hydrogensulfate (0.139 g, 0.41 mmol). With vigorous stirring a solution of 2-bromoacetophenone (16.16 g, 81.2 mmol) is added dropwise over a period of 45 min. The mixture is allowed to stir overnight. The layers are then separated and the organic layer is washed with 1N NaOH (500 mL) and water (2×300 mL), dried over magnesium sulfate and concentrated. Column chromatography (400 g silica gel) using ethyl acetate/hexane (20/80) as eluent gave 8.96 g (49%) of 7-methyl-3-phenyl-2H-1,4-benzoxazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06932961B1
Source datasetuspto-grants-2005_08
ORD IDord-52f066ce07e3455d9be8871aa7dfda8a
Source noteuspto-grants-2005_08