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benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate → (2R)-5-methoxy-2-methylpiperidine

HRID 1852756
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HRID 1852756 반응식
[CH3:1][O:2][CH:3]1[CH2:8][N:7](C(OCC2C=CC=CC=2)=O)[C@H:6]([CH3:19])[CH2:5][CH2:4]1.[H][H]>C(OCC)(=O)C.[Pd]>[CH3:1][O:2][CH:3]1[CH2:8][NH:7][C@H:6]([CH3:19])[CH2:5][CH2:4]1
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참가 물질

5

반응물 2

HCID 86724501benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 86724502(2R)-5-methoxy-2-methylpiperidine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

To benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate (345 mg, 1.31 mmol) dissolved in ethyl acetate (6.5 mL) was added palladium on carbon (139 mg, 0.13 mmol). Hydrogen gas was added via balloon, and the reaction was stirred at room temperature for 3 hours. The mixture was filtered over celite and concentrated under reduced pressure to afford (2R)-5-methoxy-2-methylpiperidine.

후처리

  1. filtrationThe mixture was filtered over celite and
  2. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7aa14cb2067c4126ab02ed7cee83726a
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962611B2

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