Water → HCID 53966869, compound

HRID 365166Notes

Reaction equation

HRID 365166 reaction equation
[N:1]1([CH:6]([CH2:10][CH2:11][CH2:12][CH3:13])[C:7](=[O:9])[CH3:8])[CH:5]=[CH:4][N:3]=[CH:2]1.[Cl:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][C:22]=1[Cl:23])[CH:18]=O.C(=O)([O-])[O-].[K+].[K+].O>CO>[Cl:14][C:15]1[CH:16]=[C:17]([CH:18]=[CH:8][C:7](=[O:9])[CH:6]([N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)[CH2:10][CH2:11][CH2:12][CH3:13])[CH:20]=[CH:21][C:22]=1[Cl:23]

Participants

6

Procedure

2.7 g of 3-(imidazole-1-yl)-2-heptanone and 3.0 g of 3,4-dichlorobenzaldehyde were dissolved in 50 ml of methanol. While stirring this solution under cooling with ice (0°-5° C.), 2.1 g of potassium carbonate was added. Then, the mixture was stirred at the same temperature for 7 hours. The reaction mixture was poured into water and extracted with chloroform. The extraction solution was treated by a usual method, and the obtained oily product was purified by chromatography, whereby 1-(3',4'-dichlorophenyl)-4-(imidazole-1-yl)-1-octene-3-one was obtained as an oily product.

Workup

  1. additionwas added
  2. stirringThen, the mixture was stirred at the same temperature for 7 hours
  3. extractionextracted with chloroform
  4. additionThe extraction solution was treated by a usual method
  5. customthe obtained oily product was purified by chromatography

Sources & evidence

ORD record
ord-43345933dc784e9b803d500880524677
Source dataset
uspto-grants-1986_08
Patent number
US04608438

Reaction notes

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