反应 #2044998
ord-f20d24647d064614926bb3a38add50c2
反应方程式
methyl 2-chloropropionate
2-(6-Hydroxy-naphthalen-2-yl)-propionic acid methyl ester
2-(6-Methoxycarbonylmethoxy-naphthalen-2-yl)-propionic acid methyl ester
K2CO3
sodium iodide
→
8
收率 85.0%
2-[6-(1-Methoxycarbonyl-ethoxy)-naphthalen-2-yl]-propionic acid methyl ester
收率 85.0%
反应物
试剂
无
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度refluxed for 50 hours
- 2workup.DISTILLATIONAcetone was distilled off
- 3workup.ADDITIONwater (1500 ml) was added
- 4萃取Crude 8 was extracted into ethyl acetate
- 5干燥dried over Na2SO4
- 6workup.DISTILLATIONdistilled
- 7其他purified by column chromatography on silica gel
实验过程
To a mixture of 2-(6-Hydroxy-naphthalen-2-yl)-propionic acid methyl ester 7 (150 g, 652 mmol), anhydrous K2CO3 (455 gr, 3.292 mol) and sodium iodide (22.5 grams, 150 mmol) in anhydrous acetone (2000 ml) was added methyl 2-chloropropionate (107.5 g, 877 mmol) and refluxed for 50 hours. Acetone was distilled off and water (1500 ml) was added. Crude 8 was extracted into ethyl acetate, dried over Na2SO4, distilled and purified by column chromatography on silica gel using hexane as eluant to give pure 8 (175 g, 85%) as a light yellow syrup. The structure was confirmed with NMR.