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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355556Generated: October 30, 2026

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

https://huagongshe.com/reaction/355556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
Reactant1,2-EpoxybutaneHCID 7834—
ReactantLithium hydroxide, monohydrateHCID 168937—
SolventEthyl AcetateHCID 8857—
Product2-Butanol, 1-[3-(trifluoromethyl)phenoxy]-HCID 11379302—

Reaction Steps

In a bomb tube (pressurized vessel), 40.5 g of 3-hydroxybenzotrifluoride, 18.0 g of α-butylene oxide and 1.0 g of lithium hydroxide monohydrate are heated for 16 hours at 140° C. After the reaction vessel has cooled, the reaction mixture is dissolved in 200 ml of ethyl acetate, and the organic phase is washed with water and subsequently dried over sodium sulfate. After concentration, the desired product 1-(3-trifluoromethylphenoxy)-2-butanol is obtained in a yield of 54.0 g and in high purity. The product can be employed in the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05831114
Source datasetuspto-grants-1998_11
ORD IDord-987c0c0333174d99907148f34b8c1d7b
Source noteuspto-grants-1998_11