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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608916Generated: November 1, 2026

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

https://huagongshe.com/reaction/1608916

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

40.5 g of 3-hydroxybenzotrifluoride, 18.0 g of α-butylene oxide and 1.0 g of lithium hydroxide monohydrate are heated in a bomb tube (pressure reactor) for 16 hours to 140° C. After cooling the reactor, the reaction mixture is dissolved in 200 ml of ethyl acetate and the organic phase is washed with water and then dried over sodium sulfate and concentrated. 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 used in the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399545
Source datasetuspto-grants-1995_03
ORD IDord-1ba4fc9f9cad4977accb87f78a19ce60
Source noteuspto-grants-1995_03