反応 #536970

ord-e3fe8978e03448e5b19ee71f2e107697

反応方程式

O=P(Cl)(OCc1ccccc1)OCc1ccccc1
dibenzyl chlorophosphate
C1CCOC1
tetrahydrofuran
Oc1ccc(C2CCCCC2)c(O)c1
4-cyclohexylresorcinol
[H-].[Na+]
sodium hydride
O=P(OCc1ccccc1)(OCc1ccccc1)Oc1ccc(C2CCCCC2)c(OP(=O)(OCc2ccccc2)OCc2ccccc2)c1
1,3-bis(dibenzylphosphonooxy)-4-cyclohexylbenzene
収率 64.0%

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGAfter stirring at room temperature for 3 hours
  2. 2
    抽出the extraction
  3. 3
    洗浄Then, the extract was washed with saturated brine (20 ml)
  4. 4
    乾燥dried with anhydrous sodium sulfate
  5. 5
    濃縮concentrated

実験手順

To a tetrahydrofuran solution (10 ml) of 4-cyclohexylresorcinol (926 mg), sodium hydride (60% dispersion in liquid paraffin) (404 mg) was added and stirred at 0° C. for 30 minutes. Then, dibenzyl chlorophosphate (10 w/v % solution in benzene) (30 ml) was added dropwise. After stirring at room temperature for 3 hours, water (30 ml) was added to the reaction mixture, and the extraction was carried out with ethyl acetate (30 ml). Then, the extract was washed with saturated brine (20 ml), dried with anhydrous sodium sulfate and then concentrated. The residue (4.12 g) was subjected to silica gel chromatography (silica gel 90 g, chloroform to chloroform:methanol=100:1), to give 1,3-bis(dibenzylphosphonooxy)-4-cyclohexylbenzene (2.19 g, yield: 64%) as a yellow liquid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08486919B2uspto-grants-2013_07