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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282434Generated: November 1, 2026

tert-Butyl methyl ether → 4-Bromo-1-fluoro-2-fluoromethyl-3-butyn-2-yl 4-Trifluoromethylphenyl Ether

https://huagongshe.com/reaction/1282434

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
ReactantBromineHCID 24408—
Reactant1-Fluoro-2-fluoromethyl-3-butyn-2-yl 4-trifluoromethylphenyl etherHCID 18424404—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
SolventHexaneHCID 8058—
Product4-Bromo-1-fluoro-2-fluoromethyl-3-butyn-2-yl 4-Trifluoromethylphenyl EtherHCID 18424415—

Reaction Steps

An amount (13.9 g) of 1-fluoro-2-fluoromethyl-3-butyn-2-yl 4-trifluoromethylphenyl ether was dissolved in a solvent consisting of a mixture of tert-butyl methyl ether (100 ml) and tert-butyl alcohol (150 ml). To the solution under cooling with ice, potassium tert-butoxide (7.1 g) was added under a nitrogen atmosphere; after stirring for a while, bromine (3 ml) was added dropwise. After the end of the dropwise addition, the mixture was stirred for 30 minutes under stirring with ice. Hexane was added to the reaction mixture, which was then washed with water and a saturated aqueous solution of sodium chloride. The mixture was dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the titled compound (18.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455708B1
Source datasetuspto-grants-2002_09
ORD IDord-81847dd3e14447bd8eb9f9c76f73b72c
Source noteuspto-grants-2002_09