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HCID 178424364, 화합물 → 2-methyl-N-[(1R)-1-phenylethyl]cyclohexan-1-amine

HRID 62659
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HRID 62659 반응식
[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][CH2:4]/[C:3]/1=[N:8]\[C@@H:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:10]>C(O)C.[Ni]>[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]1[NH:8][C@@H:9]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 178424364HCID 178424364, 화합물

생성물 1

HCID 127142172-methyl-N-[(1R)-1-phenylethyl]cyclohexan-1-amine수율 80%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

A suspension of (1R,E)-N-(2-methylcyclohexylidene)-1-phenylethanamine (I-8a: 25 g, 116.27 mmol) and Raney-Ni (3.75 g) in ethanol (250 mL) was maintained under hydrogen atmosphere in a Parr hydrogenator using 5 bar pressure for 2 days. The reaction mixture was filtered and filtrate evaporated under reduced pressure. The crude compound was treated with ethereal HCl, and the precipitated salt was filtered, washed with cold ether and dried to afford 20 g (80%) of 2-methyl-N—((R)-1-phenylethyl)-cyclohexanamine (I-8b) as a white solid.

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후처리

  1. temperaturewas maintained under hydrogen atmosphere in a Parr hydrogenator
  2. customfor 2 days
  3. filtrationThe reaction mixture was filtered
  4. customfiltrate evaporated under reduced pressure
  5. additionThe crude compound was treated with ethereal HCl
  6. filtrationthe precipitated salt was filtered
  7. washwashed with cold ether
  8. customdried

출처 및 근거

ORD 기록
ord-350460199f344be4b1b3c00607a63c82
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447039B2

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