반응 #1178422

ord-d317d83d4d3e45079ba7bb9e3ad8776c

반응 방정식

O=[N+]([O-])C1(C(O)c2cc(Cl)cc(Cl)c2)CCCCC1
(3,5-dichloro-phenyl)-(1-nitro-cyclohexyl)-methanol
NC1(C(O)c2cc(Cl)cc(Cl)c2)CCCCC1
(1-amino-cyclohexyl)-(3,5-dichloro-phenyl)-methanol
수율 82.4%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과filtered through Celite
  2. 2
    세척The filter cake was washed with methanol (2×100 mL)
  3. 3
    기타the filtrate was evaporated to dryness
  4. 4
    workup.ADDITIONThe residue was treated with 5% aqueous NaOH (100 mL)
  5. 5
    추출extracted with ethyl acetate (2×200 mL)
  6. 6
    건조The combined organic extracts were dried over Na2SO4
  7. 7
    기타evaporated

실험 절차

To a stirred solution of (3,5-dichloro-phenyl)-(1-nitro-cyclohexyl)-methanol (5.87 g, 19.3 mmol) in methanol (40 mL) and concentrated HCl (10 mL), cooled to ˜5° C., was added zinc powder. The mixture was stirred at room temperature overnight and filtered through Celite. The filter cake was washed with methanol (2×100 mL) and the filtrate was evaporated to dryness. The residue was treated with 5% aqueous NaOH (100 mL) and extracted with ethyl acetate (2×200 mL). The combined organic extracts were dried over Na2SO4 and evaporated to leave (1-amino-cyclohexyl)-(3,5-dichloro-phenyl)-methanol (4.36 g) as a white solid. 1H NMR (500 MHz, CDCl3) δ (ppm): 7.25 (s, 1H), 7.185 (s, 2H), 4.21 (s, 1H), 1.55 (m, 4H), 1.3 (m, 3H), 1.1 (m, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08129355B2uspto-grants-2012_03