反应 #302889
ord-81e7e558d5694f8490e0b682b18fc5a4
反应方程式
反应条件
后处理
- 1温度was heated
- 2温度to reflux where it
- 3温度to cool
- 4温度The reaction mixture was heated
- 5温度to reflux for about 18 hours
- 6浓缩The reaction mixture was concentrated under reduced pressure
- 7其他to leave a viscous oil residue
- 8洗涤washed with 20 mL of water
- 9萃取The organic phase was extracted with 20 mL of 3.0 molar aqueous hydrochloric acid
- 10萃取The aqueous extract
- 11workup.ADDITIONby adding 3.0 molar aqueous sodium hydroxide
- 12萃取the basic mixture was extracted with 50 mL of ethyl acetate
- 13干燥The extract was dried with sodium sulfate
- 14过滤filtered
- 15浓缩the filtrate concentrated under reduced pressure
实验过程
A mixture of 1.0 gram (0.0074 mole) of 2,3-dimethylbenzylamine and 0.69 gram (0.0081 mole) of 2-chloroethylisocyanate in 10 mL of 1,4-dioxane was heated to reflux where it stirred for about 18 hours. The reaction mixture was allowed to cool and an aqueous solution of sodium hydroxide (4.0 mL of a 3.0 molar solution) was added. The reaction mixture was heated to reflux for about 18 hours then allowed to cool to ambient temperature. The reaction mixture was concentrated under reduced pressure to leave a viscous oil residue. The residue was suspended in 50 mL of ethyl acetate and washed with 20 mL of water. The organic phase was extracted with 20 mL of 3.0 molar aqueous hydrochloric acid. The aqueous extract was made basic by adding 3.0 molar aqueous sodium hydroxide and the basic mixture was extracted with 50 mL of ethyl acetate. The extract was dried with sodium sulfate, filtered and the filtrate concentrated under reduced pressure to yield 0.81 gram of the title compound as an oil. The NMR spectrum was consistent with the proposed structure.