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Water → 2-Oxo-4-trifluoromethyl-piperidine-1-carboxylic acid tert-butyl ester

HRID 1360163
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HRID 1360163 반응식
[Na].[C:2]([O:6][C:7]([N:9]1[CH2:14][CH2:13][CH:12]([C:15]([F:18])([F:17])[F:16])[CH2:11][CH2:10]1)=[O:8])([CH3:5])([CH3:4])[CH3:3].[OH2:19]>C(OCC)(=O)C.[Ru]=O>[C:2]([O:6][C:7]([N:9]1[CH2:14][CH2:13][CH:12]([C:15]([F:18])([F:16])[F:17])[CH2:11][C:10]1=[O:19])=[O:8])([CH3:5])([CH3:3])[CH3:4]
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참가 물질

6

반응물 3

HCID 962WaterHCID 5360545SodiumHCID 49759149Tert-butyl 4-(trifluoromethyl)piperidine-1-carboxylate

생성물 1

HCID 669693432-Oxo-4-trifluoromethyl-piperidine-1-carboxylic acid tert-butyl ester수율 90%

시약·촉매·용매 2

HCID 178527103HCID 178527103, 화합물촉매
HCID 8857
Ethyl Acetate
용매
2회

실험 절차

2.82 g (3.2 mmol) of sodium methaperiodate (NaIO4) was dissolved in 20 mL of water, followed by addition of 117 mg (0.88 mmol) of ruthenium oxide (RuO2). To The reaction, was added a solution in which 660 mg (2.6 mmol) of 4-trifluoromethyl-piperidin-1-carboxylic acid t-butyl ester dissolved in 35 mL of ethyl acetate, followed by stirring for 2 hours and 20 minutes. The reaction solution was diluted with excess ethylacetate and washed once with water and aqueous NaCl, respectively, and then dried over anhydrous magnesium sulfate and filtered off. The filtrated solution was distilled off under reduced pressure, then the residue was purified by column chromatography (2:1 hexane:ethyl acetate) to give 0.63 g of the title compound in a yield of 90%.

후처리

  1. customTo The reaction
  2. washwashed once with water and aqueous NaCl
  3. dry with materialrespectively, and then dried over anhydrous magnesium sulfate
  4. filtrationfiltered off
  5. distillationThe filtrated solution was distilled off under reduced pressure
  6. customthe residue was purified by column chromatography (2:1 hexane:ethyl acetate)

출처 및 근거

ORD 기록
ord-afe85805d0e34822b87683244d9466e8
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879848B2

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