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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465271Generated: October 29, 2026

3-(Trifluoromethyl)phenol → 2-Butanol, 1-[3-(trifluoromethyl)phenoxy]-

https://huagongshe.com/reaction/465271

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
Reactant1,2-EpoxybutaneHCID 7834—
ReactantPotassium HydroxideHCID 14797—
SolventWaterHCID 962—
Product2-Butanol, 1-[3-(trifluoromethyl)phenoxy]-HCID 1137930295.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 3-trifluoromethylphenol (75 ml, 0.617 moles), 1,2-epoxybutane (58 ml, 0.617 moles), potassium hydroxide pellets (86%, 0.062 moles), and water (100 ml) were heated with stirring at 65° C. for four hours. At this point more 1,2-epoxybutane (58 ml, 0.617 moles) was added and stirring at 65° C. continued overnight. The reaction was allowed to cool to room temperature and the lower phase taken off and the upper phase extracted with methylene chloride (2×100 ml). The organic phases were combined and washed with 5% sodium hydroxide solution (150 ml) and water (3×150 ml). This reaction solution was dried over anhydrous magnesium sulfate and stripped under vacuo to yield 138 g of the desired alcohol, as determined by infra-red spectroscopy, mass spectrometry and nuclear magnetic resonance spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05152827
Source datasetuspto-grants-1992_10
ORD IDord-d0b65d578c22418ab8fa0b04e6fdedfa
Source noteuspto-grants-1992_10