反应 #95403

ord-71a010aa3742498d8fbca5124bc9b087

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.DISTILLATIONThe solvent is distilled off in vacuo
  2. 2
    workup.DISSOLUTIONthe residue is dissolved in ether
  3. 3
    洗涤the etheral solution is washed with distilled water
  4. 4
    其他dried
  5. 5
    workup.DISTILLATIONthe solvent is distilled off
  6. 6
    其他the residue is purified by column chromatography (adsorbent
  7. 7
    workup.ADDITIONKieselgel 60, solvent: a 10:0.1 mixture of benzene and methanol)

实验过程

1 ml of methanol saturated with hydrochloric acid is added to a solution of 1.05 g (0.0033 moles) of 3-(9-methoxy-3-hydroxy-5,9-dimethyl-decanoyl)-4-butyrolactone in 10 ml of dry methanol, and the mixture is allowed to stand at room temperature overnight. The solvent is distilled off in vacuo, the residue is dissolved in ether, the etheral solution is washed with distilled water, dried, the solvent is distilled off, and the residue is purified by column chromatography (adsorbent: Kieselgel 60, solvent: a 10:0.1 mixture of benzene and methanol). 0.54 g (52.1%) of the aimed compound are obtained; Rf =0.8 (developed with a 10:0.2 mixture of benzene and methanol).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04344959uspto-grants-1982_08