Cadmium chloride, dihydrate → HCID 86733692, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH:8][C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][CH:13]=2)=[O:10])[CH:2]=1.[Cl-:21].[Cd+2:22].[Cl-]>CO>[Cl-:21].[Cd+2:22].[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH:8][C:9]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][CH:13]=2)=[O:10])[CH:2]=1.[Cl-:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-(3-Pyridylmethyl)-3-(4-nitrophenyl)urea (2.72 g., 0.01 mole) was dissolved in 40 ml. of hot 2-methoxyethanol and filtered to give a clear solution. To this was added a filtered solution of cadmium chloride (1.83 g., 0.01 mole) in 300 ml. of hot methanol. The reaction mixture was cooled to room temperature to give an off-white precipitate, which was filtered off, washed with 2-methoxyethanol and air dried to give 3.5 g. of white-tan solid. It is a 77% yield of 1-(3-pyridylmethyl)-3-(4-nitrophenyl)urea cadmium chloride complex.
Workup
- filtrationof hot 2-methoxyethanol and filtered
- customto give a clear solution
- customto give an off-white precipitate, which
- filtrationwas filtered off
- washwashed with 2-methoxyethanol and air
- customdried
- customto give 3.5 g
Sources & evidence
- ORD record
- ord-b2f32d8dd7414188bb5fdfef61911fe7
- Source dataset
- uspto-grants-1976_07
- Patent number
- US03969357
Reaction notes
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