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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → 2-(4-Chlorophenoxy)-1-(piperazin-1-yl)ethanone

HRID 718240
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인쇄 미리보기

반응식

HRID 718240 반응식
[Cl:1][C:2]1[CH:24]=[CH:23][C:5]([O:6][CH2:7][C:8]([N:10]2[CH2:15][CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][CH2:11]2)=[O:9])=[CH:4][CH:3]=1.C(O)(C(F)(F)F)=O>ClCCl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][C:8]([N:10]2[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)=[O:9])=[CH:23][CH:24]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 50941486Tert-butyl 4-(2-(4-chlorophenoxy)acetyl)piperazine-1-carboxylate

생성물 1

HCID 10747602-(4-Chlorophenoxy)-1-(piperazin-1-yl)ethanone수율 736.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A suspension of tert-butyl 4-(2-(4-chlorophenoxy)acetyl)piperazine-1-carboxylate (example 58, 0.58 g, 0.16 mmol) in dichloromethane (8 ml) was treated dropwise at room temperature with TFA until the solid completely dissolved. The reaction mixture was stirred under nitrogen at room temperature overnight. The volatiles were evaporated to dryness, diluted with water and the solid was collected by filtration. The solid was washed with water and dried to yield the title compound as a white solid (0.30 g, 72%).

후처리

  1. dissolutioncompletely dissolved
  2. customThe volatiles were evaporated to dryness
  3. additiondiluted with water
  4. filtrationthe solid was collected by filtration
  5. washThe solid was washed with water
  6. customdried

출처 및 근거

ORD 기록
ord-d84d50050bd84c3290329c8432a044fd
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09193741B2

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