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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723906Generated: October 28, 2026

Water → 2,2-difluoro-4-methyl-7-nitro-4H-1,4-benzoxazin-3-one

https://huagongshe.com/reaction/723906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2-difluoro-7-nitro-4H-1,4-benzoxazin-3-oneHCID 21878155—
SolventDimethylformamideHCID 6228—
Product2,2-difluoro-4-methyl-7-nitro-4H-1,4-benzoxazin-3-oneHCID 21878106—

Reaction Steps

To a stirred suspension of 2,2-difluoro-7-nitro-4H-1,4-benzoxazin-3-one (WO 99/40094, 2.16 g, 9.38 mmol) in DMF (10 mL) is added K2CO3 (1.94 g, 14.07 mmol) followed by addition of MeI (0.87 mL, 14.07 mmol). The resulting solution is stirred over night at room temperature. To this reaction mixture is added water (50 mL), and the resulting solution is extracted with EtOAc (50 mL×3). The combined organic phases are washed with water (50 mL) and saline (50 mL), dried over Na2SO4 and concentrated under reduced pressure to give the title compound that is purified by passing through a short silica gel column with EtOAc (1.3 g, 57%), 1H NMR (300 MHz, DMSO) δ 8.25–8.17 (m, 2H), 7.62 (d, 1H), 3.47 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141588B2
Source datasetuspto-grants-2006_11
ORD IDord-6fd2f78d11e24e498e7a6a118a5640e8
Source noteuspto-grants-2006_11