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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911281Generated: November 2, 2026

Propargyl bromide → 1-(Prop-2-ynyloxy)-2-(trifluoromethoxy)benzene

https://huagongshe.com/reaction/1911281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Trifluoromethoxy)phenolHCID 2777299—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-(Prop-2-ynyloxy)-2-(trifluoromethoxy)benzeneHCID 23393437107.6%

Reaction Steps

To a solution of 2-trifluoromethoxyphenol (10.0 g, 56.1 mmol) in acetonitrile (120 mL) was added potassium carbonate (9.31 g, 67.4 mmol) and propargyl bromide (80% in toluene, 10.0 g, 7.70 mL, 67.4 mmol). The reaction was stirred at ambient temperature for seven days, then diluted with water (150 mL) and extracted with diethyl ether (300 mL). The organic layer was separated and concentrated to obtain the title compound (13.05 g) which was used without further purification in the next step. 1H NMR (300 MHz, CDCl3) δ 7.30-7.23 (m, 2H), 7.19-7.13 (m, 1H), 7.04-6.95 (m, 1H), 4.77 (d, J=2.4 Hz, 2H), 2.53 (t, J=2.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604053B2
Source datasetuspto-grants-2013_12
ORD IDord-154f029978d34d4c9893f1e9e39921c6
Source noteuspto-grants-2013_12