반응 #559165

ord-db3d9cd99f544b9f835beba3e5c7602e

반응 방정식

Oc1ccc(F)cc1
4-Fluorophenol
CC1(O)CCCCC1
1-methylcyclohexanol
O=S(=O)(O)O
sulfuric acid
CC1(c2cc(F)ccc2O)CCCCC1
4-fluoro-2-(1-methylcyclohexyl)phenol

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출The reaction mixture was then extracted by CH2C1-2(250 mL×3)
  2. 2
    세척The organic layer was washed with saturated a.q NaHCO3
  3. 3
    건조, dried over MgSO4
  4. 4
    기타evaporated under vacuum
  5. 5
    기타The residue was purified by column chromatography on silica gel

실험 절차

4-Fluorophenol (41.8 g, 373 mmol) and 1-methylcyclohexanol (63.8 g, 560 mmol) dissolved in 600 mL of dried CH2Cl2, were treated with concentrated sulfuric acid (98%, 22.3 mL, 418 mmol). The mixture was stirred at room temperature for 50 hours. The reaction mixture was then extracted by CH2C1-2(250 mL×3). The organic layer was washed with saturated a.q NaHCO3., dried over MgSO4, and evaporated under vacuum. The residue was purified by column chromatography on silica gel to give 4-fluoro-2-(1-methylcyclohexyl)phenol as a dark green oil—47.6 g. 1H NMR (400 MHz, CDCl3) δ 7.00 (dd, J=3.2, 11.2 Hz, 1H), 6.76-6.71 (m, 1H), 6.62-6.59 (m, 1H), 5.27 (brs, 1H), 2.13-2.07 (m, 2H), 1.70-1.37 (m, 8H), 1.32 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08633189B2uspto-grants-2014_01