反应 #2460304

反应方程式

1,3-dicyclohexyl-carbodiimide

1-napthoic acid

2-hydroxyethylmethacrylate

dimethylamino-pyridine p-toluenesulfonic acid salt

→

2-(1-naphthoyloxy)ethyl methacrylate

溶剂

dichloromethane

反应条件

后处理

1. 1
   温度the reaction mixture was warmed to ambient and
2. 2
   过滤The precipitated urea by-product was filtered
3. 3
   洗涤the filtrate was washed successively with 10% aqueous HCl, 10% aqueous NaHCO3, water, and brine
4. 4
   干燥The organic layer was dried (Na2SO4)
5. 5
   浓缩concentrated
6. 6
   其他The product was purified by column chromatography
7. 7
   其他to provide 8.2 g (62% of theory) of a pale yellow oil

实验过程

A mixture of 1-napthoic acid (8.0 g, 46 mmol), 2-hydroxyethylmethacrylate (18.1 g, 139 mmol), dimethylamino-pyridine p-toluenesulfonic acid salt (5.5 g, 19 mmol), and anhydrous dichloromethane (45 mL) was cooled to 0° C. under nitrogen, and 1,3-dicyclohexyl-carbodiimide (12.5 g, 60 mmol) were added. After 15 min, the reaction mixture was warmed to ambient and stirred for 3 h. The precipitated urea by-product was filtered, and the filtrate was washed successively with 10% aqueous HCl, 10% aqueous NaHCO3, water, and brine. The organic layer was dried (Na2SO4) and concentrated to deposit a gold oil. The product was purified by column chromatography to provide 8.2 g (62% of theory) of a pale yellow oil. 1H NMR (CDCl3): δ 1.90 (s, 3H), 1.55 (m, 2H), 1.70 (m, 2H), 5.60 (s, 1H), 6.20 (s, 1H), 7.55 (m, 3H), 7.90 (d, 1H), 8.05 (d, 1H), 8.20 (d, 1H), 8.90 (d, 1H).

来源