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1-Bromo-2-Chloroethane → 1-(2-Chloroethyl)-4-(3-chlorophenyl)piperazine

HRID 1835082
ノート
印刷プレビュー

反応式

HRID 1835082 の反応式
Cl.[Cl:2][C:3]1[CH:4]=[C:5]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1.[OH-].[Na+].Br[CH2:18][CH2:19][Cl:20]>CS(C)=O>[Cl:20][CH2:19][CH2:18][N:12]1[CH2:13][CH2:14][N:9]([C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([Cl:2])[CH:4]=2)[CH2:10][CH2:11]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 78491-Bromo-2-ChloroethaneHCID 14798Sodium HydroxideHCID 256811-(3-Chlorophenyl)piperazine monohydrochloride

生成物 1

HCID 100154081-(2-Chloroethyl)-4-(3-chlorophenyl)piperazine収率 59.6%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

A mixture of (3-chloro-phenyl)-piperazine hydrochloride (51.5 mmol) and powdered sodium hydroxide (103 mmol) in DMSO (75 mL) was treated with 2-bromo-1-chloroethane (77.2 mmol) and stirred at ambient temperature for 4 h. The reaction was poured into ice cold water (200 mL) and stirred for 0.5 h. A solid mass formed and was separated by decanting the water. The aqueous layer was extracted with dichloromethane (100 mL). The solid mass was dissolved with dichloromethane (100 mL) and the combined organics were dried with sodium sulfate, filtered and the solvent removed under vacuum. Flash chromatography (chloroform:acetone 50:1 to 20:1) yielded an oil (7.95 g) as the titled compound.

後処理

  1. stirringstirred for 0.5 h
  2. customA solid mass formed
  3. customwas separated
  4. customby decanting the water
  5. extractionThe aqueous layer was extracted with dichloromethane (100 mL)
  6. dissolutionThe solid mass was dissolved with dichloromethane (100 mL)
  7. dry with materialthe combined organics were dried with sodium sulfate
  8. filtrationfiltered
  9. customthe solvent removed under vacuum

出典と根拠

ORDレコード
ord-4ebb85a8e21b49908b44bbb6e47b5bb2
出典データセット
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06770638B2

反応ノート

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