反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 110 °C
PROCEDURE
实验过程
First, 8.22 g (115 mmol) of crotonaldehyde and 9.22 g (55.2 mmol) of benzenesulfonyl cyanide were introduced to the same reaction vessel as in Example 1. Toluene (15 ml) as the solvemnt and butanol (1.5 ml) were added, and 677 mg (5.55 mmol) of sodium perchlorate was added. Then the mixture was heated under reflux for 18 hours while agitating at an internal temperature of 110° C. in a nitrogen atmosphere, separating and removing water that was produced. After this solution was cooled to room temperature, the low-boiling components, such as solvent, etc., were removed under reduced pressure and the resulting concentrate was cooled in an ice bath to precipitate crystals. The crystals were filtered with a glass filter and washed with 10 ml of toluene that had been cooled to 5° C. or lower. Then the crystals were dried for 2 hours in vacuo to give 11.2 g of 2-benzenesulfonylpyridine as colorless crystals (purity of 98%, yield of 91% based on benzenesulfonyl cyanide).
WORKUP
后处理
- temperatureThen the mixture was heated
- temperatureunder reflux for 18 hours
- customseparating
- customremoving water that
- customwas produced
- temperatureAfter this solution was cooled to room temperature
- customthe low-boiling components, such as solvent, etc., were removed under reduced pressure
- concentrationthe resulting concentrate
- temperaturewas cooled in an ice bath
- customto precipitate crystals
- filtrationThe crystals were filtered with a glass
- filtrationfilter
- washwashed with 10 ml of toluene that
- temperaturehad been cooled to 5° C.
- customThen the crystals were dried for 2 hours in vacuo