반응 #2348110
ord-795cf151034845a4ac043124c056d6c5
반응 방정식
반응 조건
후처리
- 1기타Placed in a 2000-mL flask
- 2기타equipped with a stirrer
- 3workup.STIRRINGby further stirring for 10 min
- 4온도The mixture was then cooled to −17° C.
- 5workup.ADDITIONwas added dropwise to the mixture over the period of 1 hour
- 6workup.ADDITIONAfter completion of the dropwise addition
- 7workup.STIRRINGstirring
- 8workup.WAITwas continued at the same temperature for 6 hours
- 9workup.ADDITIONwas added to the reaction mixture
- 10기타for quenching
- 11기타After separation
- 12세척the organic layer was washed with water (5 times)
- 13농축the resultant organic layer was concentrated under reduced pressure
- 14기타to give 4.93 g of a crude product
- 15기타The 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.