Potassium Hydroxide → (2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutane

HRID 1823665Notes

Reaction equation

HRID 1823665 reaction equation
[OH-].[K+].[C:3]([NH:13][C@@H:14]([CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C@H:15]([OH:18])[CH2:16]Cl)([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4]>C(O)C>[CH2:6]([O:5][C:3]([NH:13][C@@H:14]([CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C@@H:15]1[O:18][CH2:16]1)=[O:4])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

Participants

4

Procedure

To a solution of 1.2 equiv. of potassium hydroxide in 968 mL of absolute ethanol at room temperature, is added 0.097 mol of N-CBZ-3(S)-amino-1-chloro-4-phenyl-2(s)-butanol. After stirring for fifteen minutes, the solvent is removed under reduced pressure and the solids are dissolved in methylene chloride. After washing with water, drying over magnesium sulfate, filtering and stripping, one obtains a white solid. Recrystallization from hot ethyl acetate and hexane will afford N-benzyloxycarbonyl-3(S)-amino-1,2(S)-epoxy-4-phenylbutane.

Workup

  1. customthe solvent is removed under reduced pressure
  2. dissolutionthe solids are dissolved in methylene chloride
  3. washAfter washing with water
  4. dry with materialdrying over magnesium sulfate
  5. filtrationfiltering
  6. customone obtains a white solid
  7. customRecrystallization from hot ethyl acetate and hexane

Sources & evidence

ORD record
ord-a2ad50264a1f46679a9b7e6aef3e3e3d
Source dataset
uspto-grants-2006_05
Patent number
US07038084B2

Reaction notes

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