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4-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidine → 4-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidin-2-one

HRID 1739003
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HRID 1739003 반응식
[C:1]([O:4][CH2:5][CH2:6][CH:7]1[CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:9][CH2:8]1)(=[O:3])[CH3:2].I([O-])(=O)(=O)=[O:21].[Na+]>C(OCC)(=O)C.O.[Ru](=O)(=O)(=O)=O>[C:1]([O:4][CH2:5][CH2:6][CH:7]1[CH2:8][CH2:9][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[C:11](=[O:21])[CH2:12]1)(=[O:3])[CH3:2]
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참가 물질

6

반응물 2

HCID 218400164-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidineHCID 23667635Sodium periodate2회

생성물 1

HCID 218400254-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidin-2-one

시약·촉매·용매 3

HCID 119079Ruthenium tetroxide촉매HCID 962Water용매2회
HCID 8857
Ethyl Acetate
용매

실험 절차

The product from Step B (0.275 g, 1.01 mmol) was dissolved in ethyl acetate (5 mL). A solution of sodium periodate in water (0.5 g in 5 mL) and ruthenium tetroxide (13 mg, 0.10 mmol) was added, and the heterogeneous reaction stirred vigorously overnight at room temperature. An additional portion of sodium periodate in water was added (0.5 g in 5 mL) and the reaction stirred overnight. The reaction was quenched with 10% sodium thiosulfate, and filtered through celite. The phases were separated, and the organic phase dried over magnesium sulfate. Filtration and evaporation gave the title compound.

후처리

  1. customthe heterogeneous reaction
  2. stirringthe reaction stirred overnight
  3. customThe reaction was quenched with 10% sodium thiosulfate
  4. filtrationfiltered through celite
  5. customThe phases were separated
  6. dry with materialthe organic phase dried over magnesium sulfate
  7. filtrationFiltration and evaporation

출처 및 근거

ORD 기록
ord-e9f33ce16e3a4a5a9567fa8dacac5ba3
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05965578

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