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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414634Generated: October 30, 2026

Water → 7-Fluoro-6-nitro-4-(prop-2-yn-1-yl)-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/414634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
Reactant7-Fluoro-6-nitro-2H-1,4-benzoxazin-3(4H)-oneHCID 13731297—
SolventDimethylformamideHCID 6228—
Product7-Fluoro-6-nitro-4-(prop-2-yn-1-yl)-2H-1,4-benzoxazin-3(4H)-oneHCID 1373129969.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of sodium hydride (0.06 g) in N,N-dimethylformamide (3 ml) was cooled to 0° C. 7-Fluoro-6-nitro-2H-1,4-benzoxazin-3(4H)-one (0.57 g) was added thereto at 0° to 5° C., and the resultant mixture was stirred for 30 minutes. Propargyl bromide (0.35 g) was added to the mixture, which was gradually heated to room temperature, and the reaction was continued for 6 hours. After addition of water, the resultant mixture was extracted with ethyl acetate, and the extract was washed with water, dried and concentrated. The residue was purified by silica gel thin layer chromatography using a mixture of ethyl acetate and n-hexane (1:1) as an eluent to give 7-fluoro-6-nitro-4-(2-propynyl)-2H-1,4-benzoxazin-3(4H)-one (0.47 g). m.p., 109.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792605
Source datasetuspto-grants-1988_12
ORD IDord-662e4e0cf5bd40b5a79ce587880ff22b
Source noteuspto-grants-1988_12