반응 #312596
ord-0b38954638cb43e1a2c5dcf9e6cba5c0
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반응 조건
후처리
- 1workup.ADDITIONwas added
- 2workup.STIRRINGAfter the reaction mixture was stirred at 40° C. for further 10 hours
- 3기타to the reaction liquid at 40° C.
- 4workup.STIRRINGlower with stirring
- 5workup.WAITAfter left
- 6기타an organic layer was separated
- 7세척the resulting organic layer was washed twice with water (100 g)
- 8workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 9기타to obtain a crude epoxide (83.8 g)
- 10workup.DISTILLATIONThe epoxide was distilled with a Claisen distiller
실험 절차
Into a 500 mL 4 necked flask equipped with a stirrer and a reflux condenser, NaWO4·2H2O (6.60 g, 0.02 mol), NaHSO4·H2O (6.90 g, 0.05 mol), [(Oct)3MeN]Cl (4.04 g, 0.01 mol), 85% H3PO4 (0.98 g, 0.0085 mol), toluene (77 g) and water (10 g) were charged. After adjusting pH of the solution to 4.0 with a 20% NaOH aqueous solution (5.8 g), L-isopulegol (77.1 g, 0.5 mol) was added thereto, and a 30% H2O2 aqueous solution (85 g, 0.75 mol) was added drop-wise at a temperature in a range of 35 to 40° C. for 1.5 hours with stirring. After the reaction mixture was stirred at 40° C. for further 10 hours, a 20% sodium sulfite aqueous solution (161 g, 0.26 mol) was added drop-wise to the reaction liquid at 40° C. or lower with stirring. After left for standing, an organic layer was separated, and the resulting organic layer was washed twice with water (100 g), and then the solvent was distilled off under reduced pressure to obtain a crude epoxide (83.8 g). The epoxide was distilled with a Claisen distiller to obtain 71.0 g of isopulegol epoxide (GC purity: 95.6%, boiling point: 93° C./533 Pa). Yield was 83% based on isopulegol.