反应 #81768

ord-4a457aa6459c470db51614492bea822a

反应方程式

O=C([O-])[O-].[K+].[K+]
potassium carbonate
Oc1c(I)cc(I)cc1I
2,4,6-triiodophenol
BrC1CCCC1
cyclopentyl bromide
Ic1cc(I)c(OC2CCCC2)c(I)c1
amber oil
收率 107.9%
Ic1cc(I)c(OC2CCCC2)c(I)c1
2,4,6-Triiodophenoxycyclopentane
收率 107.9%

反应条件

温度
130°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Milled
  2. 2
    干燥of dry (4A sieves) dimethylformamide at room temperature
  3. 3
    温度After cooling
  4. 4
    过滤the mixture was filtered
  5. 5
    洗涤the collected solid was washed with chloroform
  6. 6
    浓缩The filtrate was concentrated in vacuo

实验过程

Milled, anhydrous potassium carbonate (14.2 g, 103 mmol, 1.2 eq) was added in portions to a stirred solution of 2,4,6-triiodophenol (40.5 g, 85.8 mmol) in 50 ml of dry (4A sieves) dimethylformamide at room temperature. After stirring for 20 minutes, cyclopentyl bromide (12 ml, 112 mmol, 1.3 eq) in dimethylformamide (20 ml) was added and the viscous mixture was gradually heated to 130° C. under argon for approximately 45 minutes. After cooling, the mixture was filtered and the collected solid was washed with chloroform. The filtrate was concentrated in vacuo to give 50 g of an amber oil The crude oily product was partitioned between ethyl acetate (300 ml) and water (500 ml); the organic layer was dried over magnesium sulfate and passed through a short pad of silica gel. The filtrate was treated with decolorizing carbon, filtered, and stripped to give an amber oil. The oil was dried at 60° C. under high vacuum to give 40.4 g (87%) of product.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05620677uspto-grants-1997_04