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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243220Generated: November 1, 2026

Toluene → 8-Fluoro-5-nitro-3,4-dihydro-2H-benzo[1,4]oxazine

https://huagongshe.com/reaction/243220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTrifluoroacetic acidHCID 6422—
Reactant[2-(2,6-Difluoro-3-nitrophenoxy)ethyl]carbamic acid tert-butyl esterHCID 68157111—
SolventDichloromethaneHCID 6344—
Product8-Fluoro-5-nitro-3,4-dihydro-2H-benzo[1,4]oxazineHCID 6815767889.1%

Reaction Steps

To an ice-cold solution of [2-(2,6-difluoro-3-nitrophenoxy)ethyl]carbamic acid tert-butyl ester (450 mg, 1.416 mmol) in DCM (20 mL) was added TFA (4 mL). The reaction mixture was stirred at RT for 2.5 h, then toluene was added and volatiles were removed under reduced pressure. The resulting residue was dissolved in acetonitrile (10 mL), 2M Na2CO3 (10 mL) was added and the mixture stirred at RT for 1 h. The reaction mixture was partitioned between EtOAc and brine, the organic phase was dried (Na2SO4) and concentrated in vacuo. The residue was purified by column chromatography (Si—PCC, eluant 10-30% EtOAc in cyclohexane) affording the title compound as an orange solid (250 mg, 89%). 1H NMR (CDCl3, 300 MHz): 7.94 (1H, bs), 7.78 (1H, dd, J=9.7, 5.4 Hz), 6.45 (1H, t, J=9.5 Hz), 4.31 (2H, t, J=4.6 Hz), 3.70-3.66 (2H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-f802b4173c9a4781b961a54e3d00029d
Source noteuspto-grants-2014_02