2,6-Difluorobenzoyl isocyanate → 1-[3-Chloro-4-(2,4-dimethylphenoxy)-2,5-dimethylphenyl]-3-(2,6-difluorobenzoyl)-urea

HRID 37323

反応式

HRID 37323 の反応式
[CH3:1][C:2]1[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][C:3]=1[O:4][C:5]1[C:11]([CH3:12])=[CH:10][C:8]([NH2:9])=[C:7]([CH3:13])[C:6]=1[Cl:14].[F:20][C:21]1[CH:31]=[CH:30][CH:29]=[C:28]([F:32])[C:22]=1[C:23]([N:25]=[C:26]=[O:27])=[O:24]>C1(C)C=CC=CC=1.CCCCCC>[Cl:14][C:6]1[C:7]([CH3:13])=[C:8]([NH:9][C:26]([NH:25][C:23](=[O:24])[C:22]2[C:28]([F:32])=[CH:29][CH:30]=[CH:31][C:21]=2[F:20])=[O:27])[CH:10]=[C:11]([CH3:12])[C:5]=1[O:4][C:3]1[CH:15]=[CH:16][C:17]([CH3:19])=[CH:18][C:2]=1[CH3:1]

参加物

5

反応物 2

HCID 27333692,6-Difluorobenzoyl isocyanateHCID 148206063-Chloro-4-(2,4-dimethylphenoxy)-2,5-dimethylaniline

生成物 1

HCID 146260521-[3-Chloro-4-(2,4-dimethylphenoxy)-2,5-dimethylphenyl]-3-(2,6-difluorobenzoyl)-urea

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒2 回HCID 8058Hexane溶媒

反応条件

温度
50 °C

実験手順

Into a solution of 4-(2,4-dimethylphenoxy)-2,5-dimethyl-3-chloroaniline (1.75 grams, 6.3 mmol) prepared in Part B in 7 milliliters of toluene, which solution was warmed to a temperature of 50° C., was added 1.14 grams (6.2 mmol) of 2,6-difluorobenzoyl isocyanate in 1.5 milliliters of toluene. The reaction mixture was heated to a temperature of 90° C. and maintained at this temperature for 0.5 hours. After cooling to room temperature, the reaction mixture was diluted with 20 milliliters of hexane and then cooled in an ice bath. A precipitate formed which was collected by filtration and washed with a cold solution of 50% hexane in toluene. After vacuum drying, a white solid (1.26 grams) which was identified as 1-[3-chloro-4-(2,4-dimethylphenoxy)-2,5-dimethylphenyl]-3-(2,6-difluorobenzoyl)urea was obtained having a melting point of 183° C.-185° C. Elemental analysis of the white solid indicated the following:

後処理

  1. temperatureThe reaction mixture was heated to a temperature of 90° C.
  2. temperaturemaintained at this temperature for 0.5 hours
  3. temperatureAfter cooling to room temperature
  4. temperaturecooled in an ice bath
  5. customA precipitate formed which
  6. filtrationwas collected by filtration
  7. washwashed with a cold solution of 50% hexane in toluene
  8. customAfter vacuum drying
  9. customwas obtained

出典と根拠

ORDレコード
ord-18c1782e1b304e80ae3a4d9b3612cd5f
出典データセット
uspto-grants-1995_05
特許番号
US05420163

関連ノート

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