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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Piperidine → 5-(Piperidin-1-yl)-2,3-dihydro-1H-inden-1-one

HRID 656436
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인쇄 미리보기

반응식

HRID 656436 반응식
F[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[CH2:6][CH2:5]2.[NH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1>N1C=CC=CC=1>[N:12]1([C:2]2[CH:3]=[C:4]3[C:8](=[CH:9][CH:10]=2)[C:7](=[O:11])[CH2:6][CH2:5]3)[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8082PiperidineHCID 1365375-Fluoro-1-indanone

생성물 1

HCID 222283835-(Piperidin-1-yl)-2,3-dihydro-1H-inden-1-one

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

5-Fluoroindan-1-one (5 g, 33.3 mmol) and piperidine (8.52 g, 100 mmol, 10 ml) were dissolved in pyridine (20 ml) and heated to reflux for 3 hours. The reaction mixture was cooled, the solvent removed under vacuum, and the residue taken in diethyl ether. The ether solution was washed with 1N aqueous sodium hydroxide and with water, dried with magnesium sulfate, filtered, and the filtrate was removed under vacuum to provide the title compound which was used without further purification.

후처리

  1. temperatureheated
  2. temperatureto reflux for 3 hours
  3. temperatureThe reaction mixture was cooled
  4. customthe solvent removed under vacuum
  5. washThe ether solution was washed with 1N aqueous sodium hydroxide and with water
  6. dry with materialdried with magnesium sulfate
  7. filtrationfiltered
  8. customthe filtrate was removed under vacuum

출처 및 근거

ORD 기록
ord-e725bb48ddc94ee48416fbed064d7f43
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071762B2

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