Benzyl Chloride → HCID 178420436, compound
Reaction equation
[SH:1][C:2]1[N:6]=[CH:5][NH:4][N:3]=1.C[O-].[Na+].[CH2:10](Cl)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>CO>[CH2:10]([S:1][C:2]1[N:6]=[CH:5][NH:4][N:3]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 5 °C
Procedure
A solution of 30 g (0.29 m) 3-mercapto-1,2,4-triazole in 300 ml of dry methanol containing 16.0 g (0.29 m) sodium methoxide is stirred under dry conditions, cooled to 5° C. and benzylchloride 41.3 g (0.32 m) is added dropwise. Stir the mixture at room temperature overnight, reflux 2 hours, cool and evaporate to dryness. The residue is stirred in water and the product is extracted with ethyl acetate. Dry the ethyl acetate layer and evaporate to dryness to give white product. Recrystallize from toluene-hexane, white crystals, 41.4 g (73%), m.p. 79°-80° C.
Workup
- temperaturereflux 2 hours
- temperaturecool
- customevaporate to dryness
- stirringThe residue is stirred in water
- extractionthe product is extracted with ethyl acetate
- dry with materialDry the ethyl acetate layer
- customevaporate to dryness
- customto give white product
- customRecrystallize from toluene-hexane, white crystals, 41.4 g (73%), m.p. 79°-80° C.
Sources & evidence
- ORD record
- ord-c6dbc6b8310d478d8e62b4f0686ef1c7
- Source dataset
- uspto-grants-1982_12
- Patent number
- US04363915
Reaction notes
Loading…