反应 #577219

ord-64c126458c8142878265339f4570ce1d

反应方程式

C=CCBr
3-Bromo-1-propene
Cc1cc(=O)oc2cc(O)ccc12
7-hydroxy-4-methylcoumarin
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C=CCOc1ccc2c(C)cc(=O)oc2c1
2
收率 96.2%
C=CCOc1ccc2c(C)cc(=O)oc2c1
7-Allyloxy-4-methylcoumarin
收率 96.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The resulting mixture was then refluxed for 4 h
  2. 2
    温度to cool
  3. 3
    过滤the K2CO3 filtered off
  4. 4
    洗涤washed with fresh acetone
  5. 5
    其他The solvent was removed in vacuo
  6. 6
    其他the residue was crystallized from methanol

实验过程

3-Bromo-1-propene (2.95 mL, 34.06 mmol) was added dropwise under argon to a stirred mixture of 7-hydroxy-4-methylcoumarin 1 (2.0 g, 11.35 mmol) and anhydrous potassium carbonate (K2CO3) (2.35 g, 17.03 mmol) in acetone (50 mL). The resulting mixture was then refluxed for 4 h, after which it was allowed to cool, and the K2CO3 filtered off and washed with fresh acetone. The solvent was removed in vacuo and the residue was crystallized from methanol to afford 2 as white-cream crystals (2.36 g, 96%). TLC (hexane/ethyl acetate, 1:3): Rf=0.63. mp 110° C. 1H NMR (CDCl3, 500 MHz) δ 2.39 (s, 3H, CH3), 4.60 (d, J=5.0 Hz, 2H, CH2), 5.33 (d, J=10.5 Hz, 1H), 5.44 (d, J=17.5 Hz, 1H), 6.05 (m, 1H), 6.12 (s, 1H), 6.80 (s, 1H), 6.87 (dd, J=1.5, 9.0 Hz, 1H), 7.49 (d, J=9.0 Hz, 1H). 13C NMR (CDCl3, 125 MHz) δ 18.70, 69.29, 101.84, 112.05, 112.79, 113.75, 118.51, 125.64, 132.31, 152.61, 152.26, 161.26, 161.65. ESIMS calcd for C13H13O3 [M+H]+ 217.1, found 217.1.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07527934B2uspto-grants-2009_05