반응 #2006440

ord-bfa0d50a9d7d44b08360ddf22599e87f

반응 방정식

[Li][CH2]CCC
n-butyllithium
C=C(C)C(=O)Cl
methacryloyl chloride
O=C([O-])O.[Na+]
sodium bicarbonate
OC1(C2CCCC2)CCCC1
1-cyclopentyl-1-cyclopentanol
C=C(C)C(=O)OC1(C2CCCC2)CCCC1
title compound
수율 91.0%
C=C(C)C(=O)OC1(C2CCCC2)CCCC1
1-Cyclopentylcyclopentyl methacrylate
수율 91.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a 1-L 3-necked round bottom flask equipped with a 250-mL pressure
  2. 2
    workup.ADDITIONaddition funnel, a nitrogen inlet with thermocouple and an overhead stirrer
  3. 3
    workup.ADDITIONwas then added slowly
  4. 4
    온도with cooling over 1.5 hours
  5. 5
    workup.ADDITIONwas carefully added
  6. 6
    workup.STIRRINGThe mixture was stirred for 1 hour at which time it
  7. 7
    세척the organics washed with water, brine
  8. 8
    건조dried for 1 hour over anhydrous magnesium sulfate
  9. 9
    여과Filtration and removal of the solvent at reduced pressure
  10. 10
    기타resulted in a light-colored oil which
  11. 11
    세척was eluted with hexane through a column of 600 g of silica gel
  12. 12
    기타The UV active fractions were collected
  13. 13
    기타the solvent removed at reduced pressure

실험 절차

To a 1-L 3-necked round bottom flask equipped with a 250-mL pressure equalizing addition funnel, a nitrogen inlet with thermocouple and an overhead stirrer was added 56 g (0.364 mol) of 1-cyclopentyl-1-cyclopentanol and 400 mL of anhydrous tetrahydrofuran. The addition funnel was charged with 250 mL (0.4 mol) of n-butyllithium (1.6M in hexane) which was then added to the cooled alcohol over 2 hours. The addition funnel was then charged with a solution of 41 g (0.39 mol) of freshly distilled methacryloyl chloride in 100 mL of dry tetrahydrofuran which was then added slowly with cooling over 1.5 hours. The reaction mixture was allowed to warm to room temperature with stirring overnight after which 100 mL of saturated sodium bicarbonate was carefully added with stirring. The mixture was stirred for 1 hour at which time it was diluted with 1 L of diethyl ether and the organics washed with water, brine and dried for 1 hour over anhydrous magnesium sulfate. Filtration and removal of the solvent at reduced pressure resulted in a light-colored oil which was eluted with hexane through a column of 600 g of silica gel. The UV active fractions were collected and the solvent removed at reduced pressure to yield 74 g (91%) of the title compound as a clear, colorless oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08168366B2uspto-grants-2012_05