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Iodine → 1-[(3,4-Dihydro-2-naphthalenyl)methyl]-4-oxopiperidine

HRID 2072476
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인쇄 미리보기

반응식

HRID 2072476 반응식
[NH:1]1[CH2:6][CH2:5][C:4](=[O:7])[CH2:3][CH2:2]1.Cl[CH2:9][C:10]1[CH2:19][CH2:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=1.C(=O)([O-])[O-].[Na+].[Na+].II>C(Cl)Cl>[CH:11]1[C:12]2[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:18][CH2:19][C:10]=1[CH2:9][N:1]1[CH2:6][CH2:5][C:4](=[O:7])[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 807IodineHCID 10340Sodium CarbonateHCID 337214-PiperidoneHCID 127714333-(Chloromethyl)-1,2-dihydronaphthalene

생성물 1

HCID 214082251-[(3,4-Dihydro-2-naphthalenyl)methyl]-4-oxopiperidine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 4-piperidone (2.2 g), 3,4-dihydro-2-chloromethylnaphthalene (4.0 g), and powdered sodium carbonate (3.5 g) in tolune (200 ml) containing several crystals of iodine is refluxed for 14 hours with vigorous stirring under nitrogen. The reaction mixture is then cooled, diluted with methylene chloride (100 ml), and filtered. The filtrate is concentrated and the crude product triturated with 1:1 hexane/ether (100 ml) to give the title compound.

후처리

  1. temperatureis refluxed for 14 hours
  2. temperatureThe reaction mixture is then cooled
  3. filtrationfiltered
  4. concentrationThe filtrate is concentrated
  5. customthe crude product triturated with 1:1 hexane/ether (100 ml)

출처 및 근거

ORD 기록
ord-368f8c5c12274854af6fdcce13cb5c20
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04051248

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