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Diethylamine → 1-(4'-Chloro benzyl)-2-phenyl-4-(diethylaminoethyl) piperazine

HRID 596864
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HRID 596864 반응식
Cl.[Cl:2][C:3]1[CH:24]=[CH:23][C:6]([CH2:7][N:8]2[CH2:13][CH2:12][N:11]([CH2:14][CH2:15]Cl)[CH2:10][CH:9]2[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:5][CH:4]=1.[CH2:25]([NH:27][CH2:28][CH3:29])[CH3:26]>CC(C)=O>[Cl:2][C:3]1[CH:24]=[CH:23][C:6]([CH2:7][N:8]2[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][N:27]([CH2:28][CH3:29])[CH2:25][CH3:26])[CH2:10][CH:9]2[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8021DiethylamineHCID 70638444HCID 70638444, 화합물

생성물 1

HCID 545399441-(4'-Chloro benzyl)-2-phenyl-4-(diethylaminoethyl) piperazine

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

20 g. of 1-(4'-chloro benzyl)-2-phenyl-4-(β-chloro ethyl) piperazine hydrochloride, 14 g. of diethylamine and 200 cc. of acetone are boiled under reflux for 12 hours. After cooling, the precipitated diethylamino hydrochloride is filtered off with suction and the solvent of the filtrate is evaporated in a vacuum. The residue is distilled in a vacuum. 15 g. of a light yellow oil having a boiling point of 190° C./0.06 mm. Hg are obtained. This product is identical with the product as obtained according to Example 1 B.

후처리

  1. temperatureunder reflux for 12 hours
  2. temperatureAfter cooling
  3. filtrationthe precipitated diethylamino hydrochloride is filtered off with suction
  4. customthe solvent of the filtrate is evaporated in a vacuum
  5. distillationThe residue is distilled in a vacuum
  6. customare obtained
  7. customas obtained

출처 및 근거

ORD 기록
ord-da61dc8e8f124045a71d8124226ba79b
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04012389

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