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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | trans-1-Bromo-3-methyl-3-(4-trifluoromethylphenyl)-1-butene | HCID 15332572 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1-(2-Methylbut-3-yn-2-yl)-4-(trifluoromethyl)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05696259 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-52e07ac2bdec4ede80647a701d4be96f |
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| Source note | uspto-grants-1997_12 |
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