Potassium Iodide → 1-[(2-Methylbut-3-yn-2-yl)oxy]-4-(trifluoromethoxy)benzene
Reaction equation
[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.[CH3:13][C:14](Cl)([C:16]#[CH:17])[CH3:15].[I-].[K+].C(=O)([O-])[O-].[K+].[K+]>C(#N)C.CCCCCC.CCOCC>[CH3:13][C:14]([O:10][C:7]1[CH:6]=[CH:5][C:4]([O:3][C:2]([F:11])([F:12])[F:1])=[CH:9][CH:8]=1)([CH3:15])[C:16]#[CH:17]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of p-trifluoromethoxy phenol (30.69 g), and 2-methyl-2-chloro-3-butyne (53.00 g) in dry acetonitrile (350 mL) was added potassium iodide (14.30 g) followed by potassium carbonate (95.25 g). This reaction mixture was heated at 70°-80° C. for four days then cooled to room temperature and filtered through celite. The precipitate was washed with dichloromethane and the washing were added to the acetonitrile. The organics were evaporated in vacuo and the oil was taken up in 250 mL of dichloromethane. The organics were washed with water (2×100 mL) and dilute aqueous sodium thiosulfate (2×100 mL), dried (MgSO4), filtered and evaporated in vacuo to leave a dark brown-orange oil. Flash chromatography on SiO2 using hexane/Et2O (5/1) afforded 34.73 g of the pure product.
Workup
- temperatureThis reaction mixture was heated at 70°-80° C. for four days
- filtrationfiltered through celite
- washThe precipitate was washed with dichloromethane
- additionthe washing were added to the acetonitrile
- customThe organics were evaporated in vacuo
- washThe organics were washed with water (2×100 mL) and dilute aqueous sodium thiosulfate (2×100 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated in vacuo
- customto leave a dark brown-orange oil
Sources & evidence
- ORD record
- ord-740eabca6ce74f149ceb55c4e2856619
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04983612
Reaction notes
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