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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441013Generated: November 1, 2026

Water → 1-(2-Methylbut-3-yn-2-yl)-4-(trifluoromethyl)benzene

https://huagongshe.com/reaction/1441013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttrans-1-Bromo-3-methyl-3-(4-trifluoromethylphenyl)-1-buteneHCID 15332572—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product1-(2-Methylbut-3-yn-2-yl)-4-(trifluoromethyl)benzeneHCID 15332573—

Reaction Steps

Under a nitrogen atmosphere, a stirred solution of 40.9 grams (0.14 mole) of cis/trans-1-bromo-3-methyl-3-(4-trifluoromethylphenyl)-1-butene and 47.0 grams (0.42 mole) of potassium tert-butoxide in 300 mL of tert.butanol was heated at reflux for about three hours. After this time the reaction mixture was allowed to cool to ambient temperature as it stirred for about 18 hours. The reaction mixture was then poured into 300 mL of water and extracted with one 200 mL portion of diethyl ether. The extract was dried with magnesium sulfate, filtered, and concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel using petroleum ether as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 25.2 grams of 3-methyl-3-(4-trifluoromethylphenyl)-1-butyne. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05502054
Source datasetuspto-grants-1996_03
ORD IDord-35f6bfc0281f4283985252c3a3c9547f
Source noteuspto-grants-1996_03