Benzyl Bromide → Methylsulfinylmethylbenzylmethyl sulfonium bromide
Reaktionsgleichung
C[CH:2]([S:6][CH:7](S(C)=O)[CH3:8])[S:3]([CH3:5])=[O:4].C([Br:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[Br-:19].[CH3:5][S:3]([CH2:2][SH+:6][CH2:7][CH2:8][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:4]Komponenten
3
Versuchsvorschrift
6.21 g of methylmethylsulfinylmethyl sulfide and 17.10 g of benzyl bromide were mixed, and were then allowed to stand in reaction at 50° C. for five months. The compound obtained was washed with ether, dried at 40° C. under reduced pressure, affording a precursor, methylsulfinylmethylbenzylmethyl sulfonium bromide. Yield: 26%.
Aufarbeitung
- customto stand in reaction at 50° C. for five months
- customThe compound obtained
- washwas washed with ether
- customdried at 40° C. under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-7da4a01399a347dda8cd25e19cffa251
- Quelldatensatz
- uspto-grants-1997_06
- Patentnummer
- US05639903
Notizen zur Reaktion
Wird geladen…