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Cyclohexyl isocyanide → HCID 178482102、化合物

HRID 358264
ノート
印刷プレビュー

反応式

HRID 358264 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[CH:10][NH:11][CH:12]=2)=[CH:4][CH:3]=1.[CH:13]1([N+:19]#[C-:20])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>Cl[Cu]>[CH:13]1([NH:19][CH:20]=[N:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3[N:9]=[CH:10][NH:11][CH:12]=3)=[CH:6][CH:7]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]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

4

反応物 2

HCID 79129Cyclohexyl isocyanideHCID 178507418HCID 178507418、化合物

生成物 1

HCID 178482102HCID 178482102、化合物

試薬・触媒・溶媒 1

HCID 62652Cuprous chloride触媒

反応条件

温度
150 °C

実験手順

A mixture of 1.59 gm of 4-(p-aminophenyl)-1-H-imidazole, 1.2 gm of cyclohexyl isonitrile, and 0.99 gm of CuCl was heated at 150° C. for three hours. The thick reaction mixture was extracted with methanol. The methanol solution, after treatment with charcoal, was evaporated to dryness and extracted with ethyl acetate and 10% hydrochloric acid. The acid solution was adjusted to pH 7.5 with 17% Na2CO3 and extracted with ethyl acetate. The organic solution was evaporated to dryness. The substance remaining after recrystallization from acetone comprised 0.25 gm of the desired product.

後処理

  1. extractionThe thick reaction mixture was extracted with methanol
  2. customThe methanol solution, after treatment with charcoal, was evaporated to dryness
  3. extractionextracted with ethyl acetate and 10% hydrochloric acid
  4. extractionextracted with ethyl acetate
  5. customThe organic solution was evaporated to dryness
  6. customafter recrystallization from acetone

出典と根拠

ORDレコード
ord-d0cb2ab98ff1497aa607744d2805eefb
出典データセット
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04465841

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート