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, 10.16 g (145 mmol) of crotonaldehyde and 10.09 g (60.4 mmol) of benzenesulfonyl cyanide were introduced to the same reaction vessel as in Example 1. Toluene (15 ml) were added as the solvent, and the mixture was heated under reflux for 15 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 in vacuo for 2 hours to give 9.11 g of 2-benzenesulfonyl-pyridine as colorless crystals (purity of 90%, yield of 62% based on benzenesulfonyl cyanide).
WORKUP
后处理
- temperaturethe mixture was heated
- temperatureunder reflux for 15 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 in vacuo for 2 hours