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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184336Generated: November 1, 2026

Propargyl bromide → 2,2,7-trifluoro-6-nitro-4-(prop-2-yn-1-yl)-3,4-dihydro-2H-1,4-benzoxazin-3-one

https://huagongshe.com/reaction/1184336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,7-trifluoro-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-oneHCID 66835854—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
Product2,2,7-trifluoro-6-nitro-4-(prop-2-yn-1-yl)-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 8717388588.7%

Reaction Steps

To 2,2,7-trifluoro-6-nitro-2H-benzo[b][1,4]oxazin-3(4H)-one (6.9 g, 27.8 mmol) and potassium carbonate (4.61 g, 33.4 mmol) in dry N,N-dimethylformamide at RT was dropwise added 3-bromoprop-1-yne (80 wt % in toluene; 4.96 g, 33.4 mmol). The resulting mixture was stirred at RT overnight. The reaction mixture was poured in saturated aqueous NH4Cl solution and extracted with ethyl acetate. The combined extracts were washed with aqueous NaCl solution, dried with Na2SO4, concentrated and chased with toluene to yield 7.06 g of the title compound as a dark brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669208B2
Source datasetuspto-grants-2014_03
ORD IDord-f0210c130da542a4a1cb769b38fbfdd2
Source noteuspto-grants-2014_03