反应 #46192

ord-fc3837671c144020be731389226cb2d1

反应方程式

[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
COC(=O)C1(c2ccc(OC)cc2)CC1
methyl 1-(4-methoxyphenyl)cyclopropanecarboxylate
CCS
EtSH
COC(=O)C1(c2ccc(O)cc2)CC1
1-(4-hydroxy-phenyl)-cyclopropanecarboxylic acid methyl ester
收率 95.5%

溶剂

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added slowly at 0° C
  2. 2
    其他the organic layer was separated
  3. 3
    萃取the aqueous phase was extracted with DCM (50 mL×3)
  4. 4
    洗涤The combined organic layers were washed with H2O, brine
  5. 5
    干燥dried over Na2SO4
  6. 6
    其他evaporated under vacuum

实验过程

To a solution of methyl 1-(4-methoxyphenyl)cyclopropanecarboxylate (10.0 g, 48.5 mmol) in DCM (80 mL) was added EtSH (16 mL) under ice-water bath. The mixture was stirred at 0° C. for 20 min before AlCl3 (19.5 g, 0.15 mmol) was added slowly at 0° C. The mixture was stirred at 0° C. for 30 min. The reaction mixture was poured into ice-water, the organic layer was separated, and the aqueous phase was extracted with DCM (50 mL×3). The combined organic layers were washed with H2O, brine, dried over Na2SO4 and evaporated under vacuum to give 1-(4-hydroxy-phenyl)-cyclopropanecarboxylic acid methyl ester (8.9 g, 95%). 1H NMR (400 MHz, CDCl3) δ 7.20-7.17 (m, 2H), 6.75-6.72 (m, 2H), 5.56 (s, 1H), 3.63 (s, 3H), 1.60-1.57 (m, 2H), 1.17-1.15 (m, 2H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07741321B2uspto-grants-2010_06