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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-Cyclopentylpyridine → 3-Cyclopentylpiperidine

HRID 2212079
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반응식

HRID 2212079 반응식
[CH:1]1([C:6]2[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1>C(O)C.Cl.[Pt]=O>[CH:1]1([CH:6]2[CH2:11][CH2:10][CH2:9][NH:8][CH2:7]2)[CH2:2][CH2:3][CH2:4][CH2:5]1
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참가 물질

5

반응물 1

HCID 219638603-Cyclopentylpyridine

생성물 1

HCID 219638503-Cyclopentylpiperidine수율 84%

시약·촉매·용매 3

HCID 82844Platinum oxide (PtO)촉매HCID 313Hydrochloric Acid용매HCID 702Ethanol용매2회

실험 절차

Platinum oxide (0.2 g, 0.82 mmol) was added as a slurry in ethanol to a solution of 3-cyclopentylpyridine (1 g, 6.8 mmol) in ethanol (15 ml) and concentrated hydrochloric acid (1 ml). The mixture was hydrogenated in a Parr apparatus at 50 psi for 18 hours then filtered through Celite. The filtrate was concentrated in vacuo and the residue partitioned between 10% aqueous sodium carbonate solution and ethyl acetate. The organic layer was dried (MgSO4) and concentrated in vacuo to give the title compound (0.87 g, 84%).

후처리

  1. filtrationthen filtered through Celite
  2. concentrationThe filtrate was concentrated in vacuo
  3. customthe residue partitioned between 10% aqueous sodium carbonate solution and ethyl acetate
  4. dry with materialThe organic layer was dried (MgSO4)
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-4eda89faef2d4775ae310527e3b24da6
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07101892B2

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