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Water → (RS)-1,1-Dimethylethyl 4-(1,2-Dihydroxyethyl)-4-(phenylmethoxymethyl)-1-piperidinecarboxylate

HRID 2213031
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HRID 2213031 반응식
[CH:1]([C:3]1([CH2:16][O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)=[CH2:2].C[N+]1([O-])CC[O:29]CC1.S([O-])(O)(=O)=O.[Na+].[OH2:39]>O1CCCC1.[Os](=O)(=O)(=O)=O>[OH:39][CH:1]([C:3]1([CH2:16][O:17][CH2:18][C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:13])[CH3:14])=[O:10])[CH2:5][CH2:4]1)[CH2:2][OH:29]
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참가 물질

7

반응물 4

HCID 962WaterHCID 82029Methyl morpholine oxideHCID 516919Sodium BisulfateHCID 219553091,1-Dimethylethyl 4-Ethenyl-4-(phenylmethoxymethyl)-1-piperidinecarboxylate

생성물 1

HCID 21955196(RS)-1,1-Dimethylethyl 4-(1,2-Dihydroxyethyl)-4-(phenylmethoxymethyl)-1-piperidinecarboxylate수율 96%

시약·촉매·용매 2

HCID 30318
Osmium Tetroxide
촉매
HCID 8028Tetrahydrofuran용매

실험 절차

Osmium tetroxide (2.5 wt % solution in tert-butanol, 240 mL) was added to a mixture of 1,1-dimethylethyl 4-ethenyl-4-(phenylmethoxymethyl)-1-piperidinecarboxylate (Description 96, 1.01 g, 3 mmol) and N-methylmorpholine-N-oxide (460 mg, 4 mmol) in water (4 mL) and tetrahydrofuran (12 mL). The mixture was stirred at room temperature for 24 hours then saturated aqueous sodium hydrogen sulphate (5 mL) was added. The mixture was extracted with ethyl acetate (2×15 mL), the combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound (1.05 g, 96%). m/z (ES+) 366 (M+1).

후처리

  1. extractionThe mixture was extracted with ethyl acetate (2×15 mL)
  2. dry with materialthe combined organic fractions were dried (MgSO4)
  3. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-3be7c58a40dd4f948d7aa7f17f8a93bc
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105507B2

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