Iodobenzene → N-BOC-4-(phenylethynyl)piperidine
Reaction equation
[C:1]([CH:3]1[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)#[CH:2].I[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>C1COCC1.[Cu](I)I>[C:17]1([C:2]#[C:1][CH:3]2[CH2:4][CH2:5][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:7][CH2:8]2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Tert-butyl 4-ethynylpiperidine-1-carboxylate (12.5 g) and iodobenzene (12.8 g) was dissolved in THF:TEA=1:1 (v/v) mixed solvent (125 ml), then at room temperature, copper iodide (455 mg) and palladium tetrakistriphenylphosphine complex (1.38 g) were added thereto in that order, followed by stirring overnight at room temperature. The solvent was evaporated, EtOAc was added to it, and washed with aqueous 1 M hydrochloric acid solution, water and saturated brine in that order. This was dried over magnesium sulfate, and the solvent was evaporated to obtain a light brown oil. This was purified by silica gel column chromatography (eluent: hexane:EtOAc=19:1 (v/v)) to obtain tert-butyl 4-(phenylethynyl)piperidine-1-carboxylate (15.5 g) as a light brown oil.
Workup
- customThe solvent was evaporated
- additionEtOAc was added to it
- washwashed with aqueous 1 M hydrochloric acid solution, water and saturated brine in that order
- dry with materialThis was dried over magnesium sulfate
- customthe solvent was evaporated
- customto obtain a light brown oil
- customThis was purified by silica gel column chromatography (eluent: hexane:EtOAc=19:1 (v/v))
Sources & evidence
- ORD record
- ord-8f7984c7790c46b4aa2d618a891ae159
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07919494B2
Reaction notes
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