반응 #1311

ord-d9d51c679b094d58b2ae53013e4113f3

반응 방정식

CC1(C)CCC(Br)c2cc(Br)ccc21
4,6-dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene
CC1(C)CCC(Br)c2cc(Br)ccc21
Compound I
CC1(C)CCC(Br)c2cc(Br)ccc21
4,6-dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene
OC1CCCCC1
cyclohexanol
[Na]
sodium
[Na]
sodium
OC1CCCCC1
cyclohexanol
CC1(C)CCC(OC2CCCCC2)c2cc(Br)ccc21
title compound
CC1(C)CCC(OC2CCCCC2)c2cc(Br)ccc21
6-Bromo-4-cyclohexyloxy-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene

반응 조건

온도
70°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was cooled to ambient temperature
  2. 2
    온도The mixture was heated at 120° C. for 4 hours
  3. 3
    workup.DISTILLATIONthe excess solvent distilled off under reduced pressure
  4. 4
    workup.DISSOLUTIONThe product was dissolved in Et2O (75 ml)
  5. 5
    세척washed with water (5 ml) and brine (5 ml)
  6. 6
    건조dried over MgSO4
  7. 7
    농축concentrated in vacuo
  8. 8
    기타Purification by column chromatography (silica, 5% EtOAc-hexane)

실험 절차

To 9 g (89.9 mmol) of cyclohexanol was added 160 mg (7.0 mmol) of sodium metal and the mixture was stirred at 70° C. for 12 hours. After all of the sodium dissolved the reaction mixture was cooled to ambient temperature and then a solution of 1 g (3.2 mmol) of 4,6-dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene (Compound I) in 1 ml of cyclohexanol was added. The mixture was heated at 120° C. for 4 hours and thereafter the excess solvent distilled off under reduced pressure. The product was dissolved in Et2O (75 ml), washed with water (5 ml) and brine (5 ml), dried over MgSO4 and concentrated in vacuo. Purification by column chromatography (silica, 5% EtOAc-hexane) yielded the title compound as a colorless oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723620uspto-grants-1998_03