تفاعل #1269823
ord-b95efa034a014d89b4fb61cbb2ccf486
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىInto a 100-mL reaction vessel
- 2أخرىsubjected to separation
- 3غسيلThe thus-obtained organic phase was washed four times with 10 mL of water
- 4تركيزconcentrated under a reduced pressure
الإجراء التجريبي
Into a 100-mL reaction vessel were added 2.82 g (purity: 24%, 1.74 mmol) of sodium 2-[3-(methacryloyloxy)-2,2-difluoro-n-pentanoyloxy]-1,1-difluoroethanesulfonate obtained in Preparation Example 4-1, 9 mL of water and 9 mL of chloroform. Further, 2.10 g (7.05 mmol) of triphenylsulfonium chloride was dropped into the reaction vessel at room temperature. The resulting solution was stirred for 2 hours at room temperature and subjected to separation. The thus-obtained organic phase was washed four times with 10 mL of water and concentrated under a reduced pressure. With this, 3.00 g of target triphenylsulfonium 2-[3-(methacryloyloxy)-2,2-difluoro-n-pentanoyloxy]-1,1-difluoroethanesulfonate was obtained as a colorless oily substance. The purity of the target product was 53%; and the yield of the target product was 100%.