Nickel Dichloride → HCID 86740208, compound
Reaction equation
[CH2:1]([O:8][S:9]([O-:12])(=[O:11])=[S:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Na+].Cl[Ni:15]Cl>CO>[CH2:1]([O:8][S:9]([O-:12])(=[O:11])=[S:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1.[Ni+2:15].[CH2:1]([O:8][S:9]([O-:12])(=[O:11])=[S:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium benzylthiosulphate (57.5 g) and anhydrous NiCl2 (14.2 g) were mixed in absolute methanol (150 ml) at room temperature, and the mixture was stirred for 24 hours. It was then filtered, and methanol was evaporated from the filtrate. The residue was treated with water (50 ml) to displace the residual methanol, and the resulting solution was evaporated to dryness under vacuum, at a temperature not exceeding 50° C.
Workup
- filtrationIt was then filtered
- custommethanol was evaporated from the filtrate
- additionThe residue was treated with water (50 ml)
- customthe resulting solution was evaporated to dryness under vacuum, at a temperature not
- customexceeding 50° C.
Sources & evidence
- ORD record
- ord-267de7fc99424dc2abb9e9bc65ccdd5d
- Source dataset
- uspto-grants-1985_07
- Patent number
- US04532080
Reaction notes
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