تفاعل #2128266
ord-084620c4ea8949f6b758f75178498daa
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىA glass flask equipped with a thermometer, a condenser and a dropping funnel
- 2workup.STIRRINGAfter the termination of the dropping, stirring
- 3workup.DISSOLUTIONa reaction solution was completely dissolved
- 4أخرىThe reaction solution was separated into an organic layer
- 5استخلاصby extracting the water layer with 500 ml of diisopropyl ether
- 6غسيلSubsequently, the organic layer was rinsed with 500 ml of saturated brine
- 7تجفيفby drying with anhydrous sodium sulfate
- 8workup.DISTILLATIONThereafter, a solvent was distilled off
الإجراء التجريبي
A glass flask equipped with a thermometer, a condenser and a dropping funnel was charged with 271 g (2.24 moles) of pivaloyl chloride, 360 g (2.23 moles) of 2-bromo-2,2-difluoroethanol and 1.5 L of diisopropyl ether, followed by stirring. Then, 318 g (3.14 moles) of triethylamine was added dropwise thereto, in an iced bath. After the termination of the dropping, stirring was conducted for 1 hour at room temperature. Then, the termination of the reaction was confirmed by gas chromatography. With the addition of 300 mL of water, a reaction solution was completely dissolved therein, followed by adding 500 mL of 2N hydrochloric acid thereto. The reaction solution was separated into an organic layer and a water layer, followed by extracting the water layer with 500 ml of diisopropyl ether. Subsequently, the organic layer was rinsed with 500 ml of saturated brine, followed by drying with anhydrous sodium sulfate. Thereafter, a solvent was distilled off, thereby obtaining 485 g (82% yield, 93% purity) of 2-bromo-2,2-difluoroethyl pivalate in the form of a light yellow liquid.