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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648815Generated: November 1, 2026

Water → 1-Chloro-5-fluoro-4-nitro-2-(prop-2-yn-1-yloxy)benzene

https://huagongshe.com/reaction/648815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenol, 2-chloro-4-fluoro-5-nitro-HCID 158655—
SolventAcetonitrileHCID 6342—
Product1-Chloro-5-fluoro-4-nitro-2-(prop-2-yn-1-yloxy)benzeneHCID 1328144159%

Reaction Steps

To a solution of 2-chloro-4-fluoro-5-nitrophenol (19.1 g) in acetonitrile (100 ml), there was added anhydrous potassium carbonate (8 g). After stirring at room temperature for several minutes, propargyl bromide (14 g) was added thereto, and the resultant mixture was heated under reflux for 3 hours. After being allowed to cool to room temperature, water was added thereto, and the reaction mixture was extracted with ether. The ether extract was washed with a 5% aqueous sodium hydroxide solution and water in this order, dried over anhydrous magnesium sulfate and subjected to filtration. The filtrate was concentrated under reduced pressure, and the residue was recrystallized from ethanol to obtain 13.5 g of 4-chloro-2-fluoro-5-(2-propynyloxy)nitrobenzene. M.P. 88°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736068
Source datasetuspto-grants-1988_04
ORD IDord-657fa056a27645758ac8cb4540b83a89
Source noteuspto-grants-1988_04