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Ammonium Chloride → (2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane

HRID 1368761
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HRID 1368761 반응식
[Si]([O:8][C@@H:9]([C@H:12]([NH:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH2:10]Cl)(C(C)(C)C)(C)C.CCCC[N+](CCCC)(CCCC)CCCC.[F-].[NH4+].[Cl-]>C1COCC1.O>[C:24]([O:23][C:21]([NH:20][C@@H:12]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C@@H:9]1[O:8][CH2:10]1)=[O:22])([CH3:27])([CH3:26])[CH3:25]
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참가 물질

6

반응물 3

HCID 25517Ammonium ChlorideHCID 2724141Tetrabutylammonium FluorideHCID 70014061HCID 70014061, 화합물

생성물 1

HCID 9903372(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane수율 75%

시약·촉매·용매 2

HCID 962Water용매HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

To a magnetically stirred solution of 2(S)-t-butyldimetylsilyloxy-3(R)-(t-butyloxycarbonyl)amino-1-chloro-4-phenylbutane (30.0 mg, 0.073 mmol) in THF (0.5 mL) was added a 1 M solution of TBAF in THF (0.11 mL, 0.109 mmol) at 0° C. After 10 min, stirring was continued at room temperature for 40 min. The reaction mixture was treated with sat NH4Cl (0.5 mL), diluted with water (2 mL), and extracted with EtOAc (3 mL×3). The combined organic layers were washed with brine (3 mL), dried over anhyd magnesium sulfate, filtered, and concentrated. The residue was dissolved with MeOH (0.5 mL) and treated with KOH at 0° C. Stirring was continued at room temperature for 2 h. Solvent was removed under reduced pressure, diluted with water (2 mL), and extracted with EtOAc (3 mL×3). The combined organic layers were washed with brine (3 mL), dried over anhydrous magnesium sulfate, filtered, concentrated and column-chromatographed (10% EtOAc in n-Hex) to provide 3(S)-(t-butyloxycarbonyl)amino-1,2(S)-epoxy-4-phenylbutane (14.4 mg) as a white solid.

후처리

  1. waitwas continued at room temperature for 40 min
  2. extractionextracted with EtOAc (3 mL×3)
  3. washThe combined organic layers were washed with brine (3 mL)
  4. dry with materialdried over anhyd magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. dissolutionThe residue was dissolved with MeOH (0.5 mL)
  8. additiontreated with KOH at 0° C
  9. stirringStirring
  10. waitwas continued at room temperature for 2 h
  11. customSolvent was removed under reduced pressure
  12. additiondiluted with water (2 mL)
  13. extractionextracted with EtOAc (3 mL×3)
  14. washThe combined organic layers were washed with brine (3 mL)
  15. dry with materialdried over anhydrous magnesium sulfate
  16. filtrationfiltered
  17. concentrationconcentrated
  18. customcolumn-chromatographed (10% EtOAc in n-Hex)

출처 및 근거

ORD 기록
ord-4ba7670ab1e74f8b863db3a2036d9db2
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06573388B1

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