HRID1608737

反应详情

EQUATION

反应方程式

HRID 1608737 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

To a cooled solution of alcohol 3 (710 mg, 1.56 mmol) in acetone (17 ml) was added Jones' reagent (8N-chromic acid solution, 0.77 ml). After 30 minutes, isopropanol (5 ml) was added and the mixture was poured in water and extracted three times with ethyl acetate. The organic layer was washed twice with brine, dried over magnesium sulfate and evaporated to dryness. The crude 12,13-Bis (4-methoxyphenyl)-11-pantadecenoic acid was used in the next step without purification. To its solution in anhydrous methylene chloride (4 ml) at -10° C. was added, under stirring, triisobutylamine (470 μl, 1.96 mmol) and isobutylchloroformate (280 μl, 2.1 mmol). After 40 minutes, N-methylbutylamine (1.5 ml) was added and the mixture was stirred at room temperature during 1 hour. Methylene chloride (50 ml) was added. The organic solution was washed with 1N HCl, saturated sodium bicarbonate solution and water (3X), dried on magnesium sulfate and evaporated to dryness. The residue was purified by "Flash chromatography" on silica gel (Kieselgel 60, Merck, under 0.063 mm, 50 g). Elution with a mixture of hexane-ethyl acetate (4:1 v/v) gave N-butyl, N-methyl-12,13-Bis (4-methoxyphenyl)-11-pentadecenoic amide (4), (549 mg, 68%) colorless oil; IR νmax (neat), 1640, 1600 cm-1 ; UV γmax (log ε)=230, (4.39) nm; 1H-NMR (δ, CDCl3), 0.85-0.98 (6H, m, 2--CH2CH3), 2.27 (2H, t, J=7.1 Hz, CH2CON), 2.91 and 2.96 (3H, 2s, --NCH3), 3.25-3.36 (3H, m, --NCH2 and CH3CH2CH--), 3.77 and 3.78 (6H, 2s, OCH3), 5.50 (1H, J=7.1 Hz, --C=CH--) and 6.69-7.01 (8H, m, H--Ar) ppm; MS m/e=521 (M+).

WORKUP

后处理

  1. extractionextracted three times with ethyl acetate
  2. washThe organic layer was washed twice with brine
  3. dry with materialdried over magnesium sulfate
  4. customevaporated to dryness
  5. customThe crude 12,13-Bis (4-methoxyphenyl)-11-pantadecenoic acid was used in the next step without purification
  6. additionTo its solution in anhydrous methylene chloride (4 ml) at -10° C. was added
  7. waitAfter 40 minutes
  8. stirringthe mixture was stirred at room temperature during 1 hour
  9. washThe organic solution was washed with 1N HCl, saturated sodium bicarbonate solution and water (3X)
  10. customdried on magnesium sulfate
  11. customevaporated to dryness
  12. customThe residue was purified by "Flash chromatography" on silica gel (Kieselgel 60, Merck, under 0.063 mm, 50 g)
  13. washElution
  14. additionwith a mixture of hexane-ethyl acetate (4:1 v/v)