تفاعل #2006438

ord-55333795733d4a818a7b6b9c7eae79be

معادلة التفاعل

[Li][CH2]CCC
n-butyllithium
C=C(C)C(=O)Cl
methacryloyl chloride
O=C([O-])O.[Na+]
sodium bicarbonate
CCC1(O)CCCCCCC1
1-ethyl-1-cyclooctanol
C=C(C)C(=O)OC1(CC)CCCCCCC1
title compound
المردود 51.0%
C=C(C)C(=O)OC1(CC)CCCCCCC1
1-Ethylcyclooctyl Methacrylate
المردود 51.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a 500-mL 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
    درجة الحرارةwith 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
    غسيلthe organics washed with water, brine
  8. 8
    تجفيفdried for 1 hour over anhydrous magnesium sulfate
  9. 9
    ترشيحFiltration and removal of the solvent at reduced pressure
  10. 10
    أخرىresulted in a light-colored oil which
  11. 11
    workup.DISTILLATIONwas distilled twice from Na2CO3 and phenothiazine through a based-washed 15-cm Vigreux

الإجراء التجريبي

To a 500-mL 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 32.5 g (0.208 mol) of 1-ethyl-1-cyclooctanol and 100 mL of anhydrous tetrahydrofuran. The addition funnel was charged with 150 mL (0.239 mol, 15% excess) 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 25 g (0.239 mol) of freshly distilled methacryloyl chloride in 50 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 500 mL 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 distilled twice from Na2CO3 and phenothiazine through a based-washed 15-cm Vigreux to yield 24 g (51%) of the title compound (bp 84° C.@ 1 mmHg) as a clear, colorless oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08168366B2uspto-grants-2012_05