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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37123Generated: October 30, 2026

Phenacyl bromide → 3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-4-phenacyl-2H-1,4-benzoxazine

https://huagongshe.com/reaction/37123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantSodium hydrideHCID 24758—
Reactant2,2-Dimethyl-6-nitro-2H-benzo[B][1,4]oxazin-3(4H)-oneHCID 10656631—
SolventDimethylformamideHCID 6228—
Product3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-4-phenacyl-2H-1,4-benzoxazineHCID 1073589266.6%

Reaction Steps

In an argon gas stream, 2.0 g of 3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-2H-1,4-benzoxazine was added gradually to 0.4 g of 60% sodium hydride in oil in 40 ml of dry N,N-dimethylformamide. The mixture was stirred at room temperature for 1 hour and 2.68 g of phenacyl bromide was added. The mixture was stirred at room temperature for 1 hour, after which the solvent was distilled off under reduced pressure. The residue was diluted with 50 ml of water and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was chromatographed on a silica gel column and elution was carried out with methylene chloride-ethyl acetate. Recrystallization from ethyl acetate-ether gave 2.04 g of 3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-4-phenacyl-2H-1,4-benzoxazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420126
Source datasetuspto-grants-1995_05
ORD IDord-501f70b46e3f4601b7c88282c61ae676
Source noteuspto-grants-1995_05