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Potassium Hydroxide → (S)-2-((S)-1-azido-2-phenylethyl)oxirane

HRID 1080513
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HRID 1080513 반응식
[OH-].[K+].[N:3]([C@@H:6]([CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C@H:7]([OH:20])[CH2:8]OS(C1C=CC(C)=CC=1)(=O)=O)=[N+:4]=[N-:5]>C(O)C>[N:3]([C@H:6]([C@H:7]1[CH2:8][O:20]1)[CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[N+:4]=[N-:5]
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참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 117602043(S)-azido-4-phenyl-1-(p-toluenesulphonyloxy)-2(S)-butanol

생성물 1

HCID 10954320(S)-2-((S)-1-azido-2-phenylethyl)oxirane수율 65.4%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

A solution of 280 mg (5 mmol) of potassium hydroxide in 10 ml of ethanol were added to a solution of 1.37 g (3.8 mmol) of 3(S)-azido-4-phenyl-1-(p-toluenesulphonyloxy)-2(S)-butanol in 50 ml of ethanol and the mixture was stirred at room temperature for 1 hour. The mixture was then evaporated to dryness and the residue was partitioned between water and dichloromethane. The aqueous phase was back-extracted twice with dichloromethane. The organic phases were combined, dried over anhydrous magnesium sulphate and evaporated to give an oil which was purified by flash chromatography on silica gel using n-hexane/ethyl acetate (4:1) for the elution. There was obtained 0.47 g of 2(S)-[1(S)-azido-2-phenylethyl]oxirane: MS: m/e 189 [M]-.

후처리

  1. customThe mixture was then evaporated to dryness
  2. customthe residue was partitioned between water and dichloromethane
  3. extractionThe aqueous phase was back-extracted twice with dichloromethane
  4. dry with materialdried over anhydrous magnesium sulphate
  5. customevaporated
  6. customto give an oil which
  7. customwas purified by flash chromatography on silica gel
  8. washfor the elution

출처 및 근거

ORD 기록
ord-ebffdf9c5edf459b9d32080f15e9d91f
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05580999

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