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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363126Generated: November 1, 2026

3-(Trifluoromethyl)phenol → HCID 12870923, compound

https://huagongshe.com/reaction/2363126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
SolventHexaneHCID 8058—
ProductHCID 12870923HCID 12870923—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 3-trifluoromethyl phenol (4.05 g, 0.025 mol) and allyl bromide in acetone (50 mL) was added K2CO3 (3.5 g, 0.025 mol). The mixture was stirred overnight at 60° C. and was diluted with n-hexane. The solution was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by column chromatography to 1-alkyloxy-3-trifluoromethyl-benzene (4.0 mg, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691855B2
Source datasetuspto-grants-2014_04
ORD IDord-f1d4bea118764c0ca394e40cf6624c5b
Source noteuspto-grants-2014_04