反应 #48903

ord-d4277139295b4d52a08421ba5a29dc35

反应方程式

Cl
HCl
COc1ccc(C(C)=O)c(O)c1O
1-(2,3-dihydroxy-4-methoxyphenyl)ethanone
BrC1CCCC1
bromocyclopentane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1ccc(C(C)=O)c(O)c1OC1CCCC1
1-[3-(cyclopentyloxy)-2-hydroxy-4-methoxyphenyl]ethanone

溶剂

反应条件

温度
110°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度to cool to rt
  2. 2
    萃取extracted with diethyl ether (250 mL×2)
  3. 3
    其他The combined extracts were dried
  4. 4
    过滤filtered
  5. 5
    浓缩concentrated
  6. 6
    其他purified by silica gel chromatography (1:0→17:3; hexanes:ethyl acetate)

实验过程

A mixture of 1-(2,3-dihydroxy-4-methoxyphenyl)ethanone (10 g, 55 mmol), bromocyclopentane (6.0 mL, 56 mmol), potassium carbonate (15.5 g, 112 mmol), and anhydrous DMF (100 mL) was heated at 110° C. under N2 for 17 h and then allowed to cool to rt. The mixture was poured into 0.5N HCl (600 mL) and extracted with diethyl ether (250 mL×2). The combined extracts were dried, filtered, concentrated, and purified by silica gel chromatography (1:0→17:3; hexanes:ethyl acetate) to give 1-[3-(cyclopentyloxy)-2-hydroxy-4-methoxyphenyl]ethanone: MS (ESI): 251.2.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07745646B2uspto-grants-2010_06