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Ammonium Chloride → HCID 178488534、化合物

HRID 1059139
ノート
印刷プレビュー

反応式

HRID 1059139 の反応式
Br[C:2]1[N:3]=[CH:4][NH:5][CH:6]=1.C([Li])(C)(C)C.[CH3:12][O:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:16][C:15]=1[CH:26]=[O:27].[Cl-].[NH4+]>C1COCC1.CCCCC>[NH:5]1[CH:6]=[C:2]([CH:26]([C:15]2[CH:16]=[C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH:18]=[CH:19][C:14]=2[O:13][CH3:12])[OH:27])[N:3]=[CH:4]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 25517Ammonium ChlorideHCID 31596652-Methoxy-5-phenylbenzaldehydeHCID 178418306HCID 178418306、化合物HCID 178418934HCID 178418934、化合物

生成物 1

HCID 178488534HCID 178488534、化合物収率 34.3%

試薬・触媒・溶媒 2

HCID 8003Pentane溶媒
HCID 8028
Tetrahydrofuran
溶媒
2 回

反応条件

温度
-78 °C

実験手順

4-Bromo-1H-imidazole (5.20 g) was dissolved in THF (50 ml) and the mixture was cooled to −78° C. A solution (1.7 M; 50 ml) of t-butyllithium in pentane was added. The mixture was stirred at 0° C. for 1.5 h and cooled to −78° C. again. A solution (30 ml) of 4-methoxy[1,1′-biphenyl]-3-carbaldehyde (2.54 g) in THF was added, and the mixture was heated from −78° C. to room temperature and further stirred at room temperature for 24 h. Aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate. The organic layer was dried and concentrated. The residue was purified by silica gel column chomatography (eluent, dichloromethane:methanol=15:1) and recrystallized from ethyl acetate to give the title compound (1.15 g) as a colorless solid.

後処理

  1. temperaturecooled to −78° C. again
  2. temperaturethe mixture was heated from −78° C. to room temperature
  3. stirringfurther stirred at room temperature for 24 h
  4. extractionthe mixture was extracted with ethyl acetate
  5. customThe organic layer was dried
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chomatography (eluent, dichloromethane:methanol=15:1)
  8. customrecrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-65a646e8874844b48093ebae130913d2
出典データセット
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06518257B1

反応ノート

読み込み中…

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