반응 #2348110

ord-795cf151034845a4ac043124c056d6c5

반응 방정식

O=P(Oc1ccccc1)(Oc1ccccc1)Oc1ccccc1
triphenyl phosphate
[CH3][Zn][CH3]
dimethylzinc
CC(=O)OC(C)=O
acetic anhydride
O=C1C=CCCCCCCCCCCCC1
2-cyclopentadecenone
O=S(=O)(O)O
sulfuric acid
CC(=O)OC1=CC(C)CCCCCCCCCCCC1
3-methycyclopentadecene-1-yl acetate
수율 92.0%

반응 조건

온도
25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Placed in a 2000-mL flask
  2. 2
    기타equipped with a stirrer
  3. 3
    workup.STIRRINGby further stirring for 10 min
  4. 4
    온도The mixture was then cooled to −17° C.
  5. 5
    workup.ADDITIONwas added dropwise to the mixture over the period of 1 hour
  6. 6
    workup.ADDITIONAfter completion of the dropwise addition
  7. 7
    workup.STIRRINGstirring
  8. 8
    workup.WAITwas continued at the same temperature for 6 hours
  9. 9
    workup.ADDITIONwas added to the reaction mixture
  10. 10
    기타for quenching
  11. 11
    기타After separation
  12. 12
    세척the organic layer was washed with water (5 times)
  13. 13
    농축the resultant organic layer was concentrated under reduced pressure
  14. 14
    기타to give 4.93 g of a crude product
  15. 15
    기타The crude product was purified by silica-gel column chromatography

실험 절차

Placed in a 2000-mL flask equipped with a stirrer, dropping funnel and thermometer were 54.3 mg (0.15 mmol) of Cu(OTf)2, 25 g of toluene and 93.1 mg (0.30 mmol) of triphenyl phosphate, and the inner atmosphere was replaced with nitrogen. After replacement with nitrogen, the mixture was stirred at 25° C. for 20 min. Then, 9 mL (18 mmol) of a toluene solution (2.0 mmol/L) of dimethylzinc was added to the mixture at 25° C., followed by further stirring for 10 min. The mixture was then cooled to −17° C., followed by addition of 1.68 g (16.5 mmol) of acetic anhydride, and 3.34 g (15 mmol) of 2-cyclopentadecenone was added dropwise to the mixture over the period of 1 hour. After completion of the dropwise addition, stirring was continued at the same temperature for 6 hours. After the reaction was completed, 32.5 g of a 5% aqueous sulfuric acid solution as cooled to 0° C. was added to the reaction mixture for quenching. After separation, the organic layer was washed with water (5 times), and the resultant organic layer was concentrated under reduced pressure to give 4.93 g of a crude product. The crude product was purified by silica-gel column chromatography to produce 3.89 g (13.8 mmol, 92% yield) of dl-3-methycyclopentadecene-1-yl acetate.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07846701B2uspto-grants-2010_12