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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939699Generated: October 30, 2026

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

https://huagongshe.com/reaction/1939699

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 numberUS05696259
Source datasetuspto-grants-1997_12
ORD IDord-52e07ac2bdec4ede80647a701d4be96f
Source noteuspto-grants-1997_12