Cadmium chloride, dihydrate → HCID 86733692, compound

HRID 918046Notes

Reaction equation

HRID 918046 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

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

  1. filtrationof hot 2-methoxyethanol and filtered
  2. customto give a clear solution
  3. customto give an off-white precipitate, which
  4. filtrationwas filtered off
  5. washwashed with 2-methoxyethanol and air
  6. customdried
  7. 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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