Water → HCID 12901378, compound
Reaction equation
[C:1]1([CH3:10])[CH:6]=[CH:5][C:4]([S:7]([O-:9])=[O:8])=[CH:3][CH:2]=1.[Na+].O.Br[CH2:14][CH2:15][CH2:16][CH2:17][Sn:18]([CH3:21])([CH3:20])[CH3:19]>[Br-].C([P+](CCCC)(CCCC)CCCCCCCCCCCCCCCC)CCC.C1(C)C=CC=CC=1>[C:1]1([CH3:10])[CH:6]=[CH:5][C:4]([S:7]([CH2:14][CH2:15][CH2:16][CH2:17][Sn:18]([CH3:21])([CH3:20])[CH3:19])(=[O:9])=[O:8])=[CH:3][CH:2]=1Participants
Procedure
Into a 125 ml single-necked round bottom flask fitted with a teflon coated magnetic stir bar and a reflux condenser was charged 4.45 g of sodium p-toluenesulfinate, 20 ml water, 10 ml toluene, 7 g of 75% 4-bromobutyltrimethylstannane and 0.44 g of tri-n-butylhexadecylphosphonium bromide. The mixture was refluxed for 2.5 hours with rapid stirring. On cooling, the organic phase was separated, dried over anhydrous magesium sulfate and stripped of solvent on a rotary evaporator. The oil residue was distilled two times through a short path distillation head. The second distillation afforded 3.3 g of 4-(p-tolylsulfonyl)butyltrimethylstannane, b.p. 136°-140° C. (1 × 10-3 mm Hg). The presence of both the sulfonyl and trimethyltin moieties was indicated by strong infrared absorption bands at 1315 cm-1, 1300 cm-1, 1142 cm-1 (--SO2 --) and 765 cm-1 [(CH3)3Sn--]. NMR spectroscopy showed the following:
Workup
- customInto a 125 ml single-necked round bottom flask fitted with a teflon coated magnetic stir bar and a reflux condenser
- temperatureThe mixture was refluxed for 2.5 hours with rapid stirring
- temperatureOn cooling
- customthe organic phase was separated
- dry with materialdried over anhydrous magesium sulfate
- customstripped of solvent on a rotary evaporator
- distillationThe oil residue was distilled two times
- distillationthrough a short path distillation head
- distillationThe second distillation
Sources & evidence
- ORD record
- ord-338f87c0537844a7bb42be527ed00e03
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03976672
Reaction notes
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