반응 #806259
ord-b93164d19668495195d8b6e481c150c9
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반응 조건
후처리
- 1기타To a 1 L flask equipped with a reflux condenser
- 2온도This mixture was heated in an oil bath
- 3기타reached 50° C.
- 4workup.ADDITIONDuring the addition
- 5온도The reaction mixture was cooled
- 6기타quenched with 400 ml of water
- 7추출extracted twice with 100 ml of toluene
- 8세척The combined organic layers were washed with 50 ml of saturated ammonium chloride and 50 ml of saturated sodium chloride
- 9기타evaporated
실험 절차
To a 1 L flask equipped with a reflux condenser and a thermometer, was added 292.5 g (2.0 mol) of 2,2,4-trimethylpentan-1,3-diol, 352.0 g (4.4 mol) of 50% aqueous NaOH, and 6.45 g (20 mmol) of tetrabutyl ammonium bromide. This mixture was heated in an oil bath and when the reaction mixture reached 50° C., 199.2 g (2.2 mol) of methallyl chloride was added drop-wise over 50 minutes. During the addition, the oil bath temperature was gradually raised to 100° C. and the reaction was continued for an additional 3 hours at 100° C. The reaction mixture was cooled, quenched with 400 ml of water, and extracted twice with 100 ml of toluene. The combined organic layers were washed with 50 ml of saturated ammonium chloride and 50 ml of saturated sodium chloride and evaporated to give 408 g of crude 1-(2-methyl-2-propenyloxy)-2,2,4-trimethylpentan-3-ol. After reduced pressure distillation (71–80° C., 3 mmHg), 377.1 g (yield 94.1%) of 1-(2-methyl-2-propenyloxy)-2,2,4-trimethylpentan-3-ol was obtained.