Imidazole → 1-(2-chloro-4-fluorophenyl)-2-(1H-imidazol-1-yl)ethanone hydrochloride

HRID 1390616ノート

反応式

HRID 1390616 の反応式
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([F:11])=[CH:7][C:6]=1[Cl:12])=[O:4].O(CC)CC.[NH:18]1[CH:22]=[CH:21][N:20]=[CH:19]1.CN(C)C=O>O>[ClH:12].[Cl:12][C:6]1[CH:7]=[C:8]([F:11])[CH:9]=[CH:10][C:5]=1[C:3](=[O:4])[CH2:2][N:18]1[CH:22]=[CH:21][N:20]=[CH:19]1

参加物

6

反応物 4

HCID 795ImidazoleHCID 3283Diethyl EtherHCID 6228DimethylformamideHCID 125933352-Chloro-4-fluorophenacyl bromide

生成物 1

HCID 203326301-(2-chloro-4-fluorophenyl)-2-(1H-imidazol-1-yl)ethanone hydrochloride

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
50 °C

実験手順

To a stirred solution of 78.7 parts of 2-bromo-1-(2-chloro-4-fluorophenyl)ethanone in 140 parts of 1,1'-oxybisethane are added carefully 106.4 parts of 1H-imidazole. Upon completion, there are added 180 parts of N,N-dimethylformamide and the whole is stirred for 2 hours at 50° C. After the addition of water, the product is extracted twice with trichloromethane. The combined extracts are washed three times with water, dried, filtered and evaporated. The residue is converted into the hydrochloride salt in 4-methyl-2-pentanone, 2,2'-oxybispropane and 2-propanol. The salt is filtered off and crystallized from a mixture of ethanol and 2,2'-oxybispropane, yielding 1.5 parts of 1-(2-chloro-4-fluorophenyl)-2-(1H-imidazol-1-yl)ethanone hydrochloride; mp. 197.4° C.

後処理

  1. extractionthe product is extracted twice with trichloromethane
  2. washThe combined extracts are washed three times with water
  3. customdried
  4. filtrationfiltered
  5. customevaporated
  6. filtrationThe salt is filtered off
  7. customcrystallized from a mixture of ethanol and 2,2'-oxybispropane

出典と根拠

ORDレコード
ord-0dd4b8396aeb493ba0b32b956272542d
出典データセット
uspto-grants-1979_02
特許番号
US04139540

反応ノート

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