반응 #1198

ord-cb6871243aa046c0acd17a0fc444cdcb

반응 방정식

CCCCCCCCCCCCCCO
tetradecanol
[H-].[Na+]
NaH
C=C(C)CCl
methallyl chloride
O=C(OO)c1cccc(Cl)c1
m-chloroperbenzoic acid
CCCCCCCCCCCCCCOCC1(C)CO1
1,2-epoxy-2-methyl-3-tetradecyloxypropane
수율 79.5%

반응 조건

온도
60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A 200-ml flask equipped with a stirrer
  2. 2
    기타After completion of the reaction
  3. 3
    추출subjected to extraction with hexane
  4. 4
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  5. 5
    workup.ADDITIONThe resultant residue was charged into a 300-ml flask
  6. 6
    기타equipped with a stirrer
  7. 7
    기타Solids formed
  8. 8
    기타were separated by filtration
  9. 9
    농축the resultant solution was concentrated under reduced pressure
  10. 10
    기타purified by column chromatography on silica gel

실험 절차

A 200-ml flask equipped with a stirrer was charged with 10 g (46.6 mmol) of tetradecanol, 50 ml of dimethylformamide, 2.86 g (71.5 mmol) of 60% NaH and 5.96 g (65.8 mmol) of methallyl chloride. The contents were stirred at 60° C. for 15 hours. After completion of the reaction, the reaction mixture was added with water and subjected to extraction with hexane, and the solvent was distilled off under reduced pressure. The resultant residue was charged into a 300-ml flask equipped with a stirrer, and 12.24 g (70.9 mmol) of m-chloroperbenzoic acid and 200 ml of dichloromethane were added thereto. The resultant mixture was stirred at room temperature for 19 hours. Solids formed were separated by filtration, and the resultant solution was concentrated under reduced pressure and then purified by column chromatography on silica gel, thereby obtaining 10.54 g (yield: 79.4%) of 1,2-epoxy-2-methyl-3-tetradecyloxypropane as an intermediate.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723497uspto-grants-1998_03