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Water → 4-Chloro-N-[(1H-imidazol-2-yl)methyl]aniline

HRID 1179437
ノート
印刷プレビュー

反応式

HRID 1179437 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]=O.[Cl:8][C:9]1[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=1.[BH4-].[Na+].O>CO>[Cl:8][C:9]1[CH:15]=[CH:14][C:12]([NH:13][CH2:6][C:2]2[NH:3][CH:4]=[CH:5][N:1]=2)=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 78124-ChloroanilineHCID 249551H-imidazole-2-carbaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 108460134-Chloro-N-[(1H-imidazol-2-yl)methyl]aniline収率 53.9%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

このページの内容参加物実験手順後処理出典と根拠反応ノート

The solution of 2-imidazolecarboxaldehyde (570 mg, 5.9 mmol) and 4-chloroaniline (756 mg, 5.9 mmol) in methanol (5 ml) was stirred at 60° C. for 4 hours, and allowed to cool to room temperature. To the reaction was added NaBH4 (337 mg, 8.9 mmol), and the mixture was additionally stirred for an hour. Water (20 mL) was added to the reaction, which was extracted with ethyl acetate (50 mL). Organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (5% methanol in chloroform) to give the title compound (660 mg, 53%).

後処理

  1. extractionwas extracted with ethyl acetate (50 mL)
  2. dry with materialOrganic layer was dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (5% methanol in chloroform)

出典と根拠

ORDレコード
ord-813eb3b18b5d45a98cf056db46d03476
出典データセット
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07279497B2

反応ノート

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