HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648724Generated: November 3, 2026
2-Methyl-3-butyn-2-ol → 4-(4-fluorophenyl)-2-methylbut-3-yn-2-ol
https://huagongshe.com/reaction/1648724
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-(4-fluorophenyl)-2-methylbut-3-yn-2-ol | HCID 5163744 | 78% |
Reaction Steps
To a solution of 35.2 g (0.19 mole) of 4-bromofluorobenzene and 25.2 g (0.3 mole) of 3-hydroxy-3-methyl-1-butine in 250 ml of triethylamine are added, under nitrogen, 1 g of the palladium complex PdCl2 [P(C6H5)3 ]2 and 0.2 g of copper(I) iodide. The reaction mixture is subsequently stirred for 24 hours at 70° C. After filtering off triethylammonium bromide and removing excess triethylamine by evaporation, the residue is taken up in 200 ml of ether and the solution is washed twice with 100 ml of 5% aqueous HCl solution and 100 ml of water, dried, treated with activated charcoal, and evaporated to dryness. The residue is chromatographed on silica gel with a 1:1 mixture of ether/hexane, affording 26.4 g (78%) of 1-fluoro-4-(3-hydroxy-3-methyl-1-butyn-1-yl)-benzene with a melting point of 124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04412856 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-2d038cce83ad48b49d4cff65137d7350 |
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| Source note | uspto-grants-1983_11 |
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