Tributylstannane → HCID 54528940, compound
Reaction equation
[CH2:1]([C:4]1([CH2:15][N:16]2[CH:20]=[CH:19][N:18]=[CH:17]2)[S:8][C:7]2[CH:9]=[C:10]([Cl:13])[CH:11]=[CH:12][C:6]=2[CH:5]1Cl)[CH:2]=[CH2:3].C([SnH](CCCC)CCCC)CCC>C1(C)C=CC=CC=1>[CH2:1]([C:4]1([CH2:15][N:16]2[CH:20]=[CH:19][N:18]=[CH:17]2)[S:8][C:7]2[CH:9]=[C:10]([Cl:13])[CH:11]=[CH:12][C:6]=2[CH2:5]1)[CH:2]=[CH2:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Heat a reaction mixture of 1.4 g (4.3 mmoles) of the title compound of Example 7 and 2.5 g (8.5 mmoles) of tri(n-butyl)tin hydride in 20 mL of toluene at reflux overnight. Evaporate to give a residue. Chromatograph the residue on silica gel, eluting with 1:1 (v/v) ethyl acetate:hexane to give the title compound as an oil, m/e 290.
Workup
- temperatureHeat
- temperatureat reflux overnight
- customEvaporate
- customto give a residue
- washChromatograph the residue on silica gel, eluting with 1:1 (v/v) ethyl acetate
Sources & evidence
- ORD record
- ord-6667037728114557b1ad67f3b10a7eb9
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04731364
Reaction notes
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