반응 #1596976
ord-9236dd49094a47558b6abc9de8560b02
반응 방정식
용매
반응 조건
후처리
- 1기타Into a 300 mL three-necked flask equipped with a gas-inlet tube, a reflux condenser
- 2온도by cooling with ice
- 3workup.ADDITIONAfter completion of the addition
- 4workup.ADDITIONafter completion of the addition
- 5workup.STIRRINGthe whole was stirred as it
- 6기타an organic layer was separated by two-layer separation in a separating funnel
- 7workup.DISTILLATIONThe resulting organic layer was subjected to distillation under normal pressure
- 8기타to collect a fraction of 106° C. to 107° C.
실험 절차
Into a 300 mL three-necked flask equipped with a gas-inlet tube, a reflux condenser, and a thermometer was charged 10.0 g (0.12 mol) of ethylene chlorohydrin beforehand, followed by cooling with ice. Then, 20.0 g (0.12 mol) of hexafluoroacetone was added through the gas-inlet tube. After completion of the addition, the whole was stirred for 15 minutes as it was and then 100 mL of t-butyl methyl ether was added. Then, 16.6 g (0.12 mol) of potassium carbonate was added portionwise over a period of 1 hour and, after completion of the addition, the whole was stirred as it was. The resulting mixture was poured into 100 mL of water and an organic layer was separated by two-layer separation in a separating funnel. The resulting organic layer was subjected to distillation under normal pressure to collect a fraction of 106° C. to 107° C. to obtain 15.8 g (purity 99%, yield 62.0%) of 2,2-bis(trifluoromethyl)-1,3-dioxolane (fluorinated acetal (E)).