반응 #48168

ord-6faa8a0bc8f0409f90583664eb3f629d

반응 방정식

CC(C)OC(=O)N=NC(=O)OC(C)C
Diisopropyl azodicarboxylate
Cc1cc(O)ccc1[N+](=O)[O-]
3-methyl-4-nitrophenol
CC(C)(C)OC(=O)N1CCC(O)CC1
1-tert-butyloxycarbonyl-4-hydroxy-piperidine
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
Cc1cc(OC2CCN(C(=O)OC(C)(C)C)CC2)ccc1[N+](=O)[O-]
4-(3-Methyl-4-nitro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the mixture was evaporated to dryness
  2. 2
    workup.DISSOLUTIONdissolved in tert-butylmethylether
  3. 3
    세척The organic phase was washed with 0.5M sodium hydroxide solution and 5% sodium chloride solution
  4. 4
    건조dried over sodium sulfate
  5. 5
    여과filtered
  6. 6
    기타evaporated to dryness
  7. 7
    기타The product was recrystallized from methanol
  8. 8
    기타to yield 9.498 g (88%) as white crystals

실험 절차

Diisopropyl azodicarboxylate (10.56 mL, 1.6 eq.) was added to a cold (0° C.) mixture of 3-methyl-4-nitrophenol (5 g, 1.0 eq.), 1-tert-butyloxycarbonyl-4-hydroxy-piperidine (9.96 g, 1.6 eq.) and triphenylphosphine (13.85 g, 1.6 eq.) in tetrahydrofuran (205 mL). After 1 h stirring, the mixture was evaporated to dryness and dissolved in tert-butylmethylether. The organic phase was washed with 0.5M sodium hydroxide solution and 5% sodium chloride solution, dried over sodium sulfate, filtered and evaporated to dryness. The product was recrystallized from methanol to yield 9.498 g (88%) as white crystals. MS (m/e): 336.2 (M, 10%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745479B2uspto-grants-2010_06