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Cyclohexene → Methyl 4-[(1-hydroxy-2-methylindolizin-3-yl)carbonyl]benzoate

HRID 1716352
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인쇄 미리보기

반응식

HRID 1716352 반응식
C1CCCCC=1.C([O:14][C:15]1[C:16]([CH3:36])=[C:17]([C:24]([C:26]2[CH:35]=[CH:34][C:29]([C:30]([O:32][CH3:33])=[O:31])=[CH:28][CH:27]=2)=[O:25])[N:18]2[C:23]=1[CH:22]=[CH:21][CH:20]=[CH:19]2)C1C=CC=CC=1>C(O)C.[Pd]>[OH:14][C:15]1[C:16]([CH3:36])=[C:17]([C:24]([C:26]2[CH:35]=[CH:34][C:29]([C:30]([O:32][CH3:33])=[O:31])=[CH:28][CH:27]=2)=[O:25])[N:18]2[C:23]=1[CH:22]=[CH:21][CH:20]=[CH:19]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8079CyclohexeneHCID 12069558Methyl 4-[(1-(benzyloxy)-2-methylindolizin-3-yl)carbonyl]benzoate

생성물 1

HCID 12069595Methyl 4-[(1-hydroxy-2-methylindolizin-3-yl)carbonyl]benzoate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

8.75 ml (86.37 mmol) of cyclohexene are added to 3.45 g (8.64 mmol) of methyl 4-[(1-(benzyloxy)-2-methylindolizin-3-yl)carbonyl]benzoate in 40 ml of ethanol, in the presence of 690 mg of 10% Pd/C, and the medium is heated under reflux for one hour.

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후처리

  1. temperaturethe medium is heated
  2. temperatureunder reflux for one hour

출처 및 근거

ORD 기록
ord-411c6c6c60b14d68bf58a0ec50278fab
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07803811B2

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