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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64694Generated: October 25, 2026

3-(Trifluoromethyl)phenol → 2-Butanol, 4-chloro-1-[3-(trifluoromethyl)phenoxy]-

https://huagongshe.com/reaction/64694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-Dichloro-2-butanolHCID 17021—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product2-Butanol, 4-chloro-1-[3-(trifluoromethyl)phenoxy]-HCID 13120348—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of 0.5 mole (75 g.) of m-trifluoromethylphenol, 1 mole (56 g.) of potassium hydroxide, 100 ml. of water and 400 ml. of isopropanol was added 0.6 mole (84 g.) of 1,4-dichloro-2-butanol with stirring at temperature below 55° C. The resulting reaction mixture was heated at 65° C. for 20 hr., mixed with 2 liters of water, and extracted with 400 ml. of isopropyl ether. The ether extract was washed with 0.5N sodium hydroxide and then with water, dried over sodium sulfate and distilled under reduced pressure. The distillate which was collected at 120°-124° C./0.01 mm. solidified at room temperature and melted at 50°-52° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609735
Source datasetuspto-grants-1986_09
ORD IDord-f451d76dd022479d86c4d6ad57a6b1ae
Source noteuspto-grants-1986_09