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Aluminium lithium hydride → 3-Benzyloxymethylcyclohexylamine

HRID 1734232
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반응식

HRID 1734232 반응식
[CH2:1]([O:8][CH2:9][CH:10]1[CH2:15][CH2:14][CH2:13][C:12](=[N:16]O)[CH2:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C(OCC)C>[CH2:1]([O:8][CH2:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH:12]([NH2:16])[CH2:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 856315583-Benzyloxymethylcyclohexanone oxime

생성물 1

HCID 153448223-Benzyloxymethylcyclohexylamine수율 86.9%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

To a solution of the compound (12) (0.75 g; 3.2 mmol) in diethyl ether (30 ml), lithium aluminum hydride (0.75 g; 20 mmol) is added, and the resultant mixture is refluxed for 3 hours. After cooling, wet ether is dropwise added to the reaction mixture, and the organic layer is collected by decantation and dried, followed by concentration under reduced pressure to give 3-benzyloxymethylcyclohexylamine (13) (0.61 g).

후처리

  1. temperatureAfter cooling
  2. customthe organic layer is collected by decantation
  3. customdried
  4. concentrationfollowed by concentration under reduced pressure

출처 및 근거

ORD 기록
ord-c8b5fe68ead14feb902225d0b685e3e0
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05532372

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