반응 #40337

ord-1b1a75c210864a4abfc772d05a463448

반응 방정식

C[Si](C)(C)OC1=CCC(c2ccccc2)CC1
Trimethyl-(4-phenyl-cyclohex-1-enyloxy)-silane
CC(C)(C)Cl
tert-butyl chloride
CC(C)(C)C1CC(c2ccccc2)CCC1=O
title compound
수율 15.0%
CC(C)(C)C1CC(c2ccccc2)CCC1=O
2-tert-butyl-4-phenyl-cyclohexanone
수율 15.0%

반응 조건

온도
-45°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONis added
  2. 2
    세척washed with ice water
  3. 3
    건조The organic phase is dried over sodium sulphate
  4. 4
    기타the solvent is removed in a vacuum

실험 절차

Trimethyl-(4-phenyl-cyclohex-1-enyloxy)-silane (7.27 mmol) and tert-butyl chloride (7.85 mmol) are introduced first in dichloromethane under nitrogen and cooled to −45° C. A solution, also cooled to −45° C., of titanium tetrachloride (7.63 mmol) in dichloromethane (3.6 ml) is added, and stirring is continued for 3 hours at this temperature. The reaction mixture is diluted with dichloromethane and washed with ice water. The organic phase is dried over sodium sulphate and the solvent is removed in a vacuum. Column chromatography (ethyl acetate/heptane 1:4) of the residue produces the title compound (250 mg) in a yield of 15% (Angew Chem Int Ed Engl 1978, 17, 1, 48-49). 1H NMR (ppm, CDCl3): 7.35 (5H); 3.15 (1H); 2.55 (1H); 2.4 (3H); 2.25 (1H); 2 (1H); 1.8 (1H); 1.05 (9H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07727979B2uspto-grants-2010_06