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Sodium Chloride → 1-Methyl-3-phenyl-4-[2-hydroxy-2-(4-chlorophenyl)ethyl]piperazine

HRID 622780
ノート
印刷プレビュー

反応式

HRID 622780 の反応式
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][C:9]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=2)=[O:10])[CH:4]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:3]1.[BH4-].[Na+].[Cl-].[Na+]>C(O)C>[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][CH:9]([OH:10])[C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=2)[CH:4]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 5234Sodium ChlorideHCID 4311764Sodium borohydrideHCID 143023441-Methyl-3-phenyl-4-(4-chlorophenacyl) piperazine

生成物 1

HCID 143023451-Methyl-3-phenyl-4-[2-hydroxy-2-(4-chlorophenyl)ethyl]piperazine収率 63.6%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a stirred solution of 25 g (0.076 mol) of the 1-methyl-3-phenyl-4-(4-chlorophenacyl) piperazine in 450 ml of ethanol was added in portions 2.9 (0.076 mol) of sodium borohydride. The resulting mixture was stirred at ambient temperature for 2 hours, poured into 50% aqueous sodium chloride and extracted with ethyl acetate. The organic extracts were combined, washed with water and saturated sodium chloride and dried over sodium sulfate. The resulting crude product obtained from concentration of the filtrate was subjected to rapid liquid chromatography on a silica gel column to give 16 g (60% overall) of 1-methyl-3-phenyl-4-[2-hydroxy-2-(4-chlorophenyl)ethyl]piperazine as a white solid.

後処理

  1. extractionextracted with ethyl acetate
  2. washwashed with water and saturated sodium chloride
  3. dry with materialdried over sodium sulfate
  4. customThe resulting crude product obtained from concentration of the filtrate

出典と根拠

ORDレコード
ord-e40b2381a4784ae5a95a81524de7bbc1
出典データセット
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04772705

反応ノート

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