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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-butyn-2-olHCID 8258—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantTriphenylphosphineHCID 11776—
CatalystPalladiumHCID 23938—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTriethylamineHCID 8471—
Product4-(4-fluorophenyl)-2-methylbut-3-yn-2-olHCID 516374478%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04412856
Source datasetuspto-grants-1983_11
ORD IDord-2d038cce83ad48b49d4cff65137d7350
Source noteuspto-grants-1983_11