Benzyl Bromide → HCID 69471538, compound
Reaction equation
[F:1][CH2:2][C:3]([NH2:5])=[S:4].[CH2:6]([Br:13])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C(Cl)(Cl)Cl.CCOCC>[BrH:13].[CH2:6]([S:4][C:3](=[NH:5])[CH2:2][F:1])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Fluorothioacetamide (3.39 g) and benzyl bromide (6.23 g) were refluxed in chloroform (40 ml), under nitrogen, for 16 h. After cooling, the mixture was diluted with ether (200 ml) and the resulting orange solid filtered off. The solid was washed with more ether and dried over P2O5 in vacuo to give 5.19 g of the desired product.
Workup
- temperatureAfter cooling
- filtrationthe resulting orange solid filtered off
- washThe solid was washed with more ether
- dry with materialdried over P2O5 in vacuo
Sources & evidence
- ORD record
- ord-93a754e113f9425abbc9ad40dd8b8ff7
- Source dataset
- uspto-grants-1999_03
- Patent number
- US05889056
Reaction notes
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