反应 #2044998

ord-f20d24647d064614926bb3a38add50c2

反应方程式

COC(=O)C(C)Cl
methyl 2-chloropropionate
COC(=O)COc1ccc2cc(C(C)C(=O)OC)ccc2c1
2-(6-Hydroxy-naphthalen-2-yl)-propionic acid methyl ester
COC(=O)COc1ccc2cc(C(C)C(=O)OC)ccc2c1
2-(6-Methoxycarbonylmethoxy-naphthalen-2-yl)-propionic acid methyl ester
O=C([O-])[O-].[K+].[K+]
K2CO3
[I-].[Na+]
sodium iodide
COC(=O)C(C)Oc1ccc2cc(C(C)C(=O)OC)ccc2c1
8
收率 85.0%
COC(=O)C(C)Oc1ccc2cc(C(C)C(=O)OC)ccc2c1
2-[6-(1-Methoxycarbonyl-ethoxy)-naphthalen-2-yl]-propionic acid methyl ester
收率 85.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度refluxed for 50 hours
  2. 2
    workup.DISTILLATIONAcetone was distilled off
  3. 3
    workup.ADDITIONwater (1500 ml) was added
  4. 4
    萃取Crude 8 was extracted into ethyl acetate
  5. 5
    干燥dried over Na2SO4
  6. 6
    workup.DISTILLATIONdistilled
  7. 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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08409559B2uspto-grants-2013_04