تفاعل #1198

ord-cb6871243aa046c0acd17a0fc444cdcb

معادلة التفاعل

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
المردود 79.5%

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 200-ml flask equipped with a stirrer
  2. 2
    أخرىAfter completion of the reaction
  3. 3
    استخلاصsubjected 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
    أخرىequipped with a stirrer
  7. 7
    أخرىSolids formed
  8. 8
    أخرىwere separated by filtration
  9. 9
    تركيزthe resultant solution was concentrated under reduced pressure
  10. 10
    أخرىpurified by column chromatography on silica gel

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723497uspto-grants-1998_03