Sulfuric Acid → 3-Methylcyclopentadecene-1-yl acetate

Temperatur

25 °C

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.

1. customPlaced in a 2000-mL flask
2. customequipped with a stirrer
3. stirringby further stirring for 10 min
4. temperatureThe mixture was then cooled to −17° C.
5. additionwas added dropwise to the mixture over the period of 1 hour
6. additionAfter completion of the dropwise addition
7. stirringstirring
8. waitwas continued at the same temperature for 6 hours
9. additionwas added to the reaction mixture
10. customfor quenching
11. customAfter separation
12. washthe organic layer was washed with water (5 times)
13. concentrationthe resultant organic layer was concentrated under reduced pressure
14. customto give 4.93 g of a crude product
15. customThe crude product was purified by silica-gel column chromatography

ORD-Eintrag

ord-795cf151034845a4ac043124c056d6c5

Quelldatensatz

uspto-grants-2010_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07846701B2