Triphenylphosphine → 1-(3-Phenylbenzo[b]thiophen-2-yl)ethanamine
Reaction equation
[N:1]([CH:4]([C:6]1[S:10][C:9]2[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=2[C:7]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH3:5])=[N+]=[N-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C1COCC1.O>[C:15]1([C:7]2[C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[S:10][C:6]=2[CH:4]([NH2:1])[CH3:5])[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
2-(1-Azidoethyl)-3-phenylbenzo[b]thiophene (211 mg, 0.76 mmol) was dissolved in a mixture THF (4 mL) and water (0.27 mL) and triphenylphosphine (237 mg, 0.91 mmol) added. The mixture was stirred at RT for 1 h then additional triphenylphosphine (237 mg) was added. The reaction mixture was stirred at RT for 1 h then the reaction mixture was loaded onto an Isolute® SCX-2 cartridge and washed with MeOH and the product eluted with 2M NH3/MeOH. The product containing fractions were combined and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-8% MeOH in DCM) affording the title compound as a white solid (160 mg, 83%). 1H NMR (CDCl3, 400 MHz): δ 7.84 (1H, dd, J=7.63, 1.55 Hz), 7.52-7.27 (8H, m), 4.56-4.44 (1H, br), 1.76 (2H, s), 1.47 (3H, d, J=6.21 Hz).
Workup
- additionadded
- stirringThe reaction mixture was stirred at RT for 1 h
- washwashed with MeOH
- washthe product eluted with 2M NH3/MeOH
- additionThe product containing fractions
- concentrationconcentrated in vacuo
- customThe resulting residue was purified by column chromatography (Si—PCC, gradient 0-8% MeOH in DCM)
Sources & evidence
- ORD record
- ord-ab83539bea0a4d948230a1791c30ac3c
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08653089B2
Reaction notes
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