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Chloroform → HCID 57602861, 화합물

HRID 1788389
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HRID 1788389 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=[CH:14][CH2:15][OH:16])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(Cl)(Cl)Cl>CCCCCC.[O-2].[O-2].[Mn+4]>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=[CH:14][CH:15]=[O:16])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6212ChloroformHCID 22594495tert-Butyl 4-(2-hydroxyethylidene)piperidine-1-carboxylate

생성물 1

HCID 57602861HCID 57602861, 화합물수율 89%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 8058Hexane용매

실험 절차

To a solution of 4-(2-hydroxyethylidene)piperidine-1-carboxylic acid t-butyl ester (10.4 g, 46 mmol) in a mixture of hexane (300 mL)-chloroform (100 mL) was added manganese dioxide (100 g), and stirred for 10 hours. After the reaction was completed, insoluble materials were filtered off through Celite and the filtrate was concentrated under a reduced pressure to obtain 9.2 g (yield 89%) of 4-(2-oxoethylidene)piperidine-1-carboxylic acid t-butyl ester (VII-18, 20, 21, 24, 30, 41, 42, 43, 44, 45).

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후처리

  1. filtrationinsoluble materials were filtered off through Celite
  2. concentrationthe filtrate was concentrated under a reduced pressure

출처 및 근거

ORD 기록
ord-837679e5d7ae48f7b6381523e1ee1665
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07511144B2

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