تفاعل #1973908

ord-a6dc42d530284376b579ab4a6f704085

معادلة التفاعل

[H][H]
hydrogen
[Li]
lithium
[H-]
hydride
COc1ccc(Cl)c(NC(=O)COCc2ccccc2)c1
2-Benzyloxy-N-(2-chloro-5-methoxy-phenyl) acetamide
[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminium hydride
COc1ccc(Cl)c(NCCOCc2ccccc2)c1
(2-Benzyloxy-ethyl)-(2-chloro-5-methoxyphenyl) amine
المردود 101.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    درجة الحرارةThe reaction was then heated
  3. 3
    درجة الحرارةto reflux for 4 h
  4. 4
    أخرىto stand at RT over the weekend
  5. 5
    أخرىThe reaction was then quenched by the dropwise addition of water (50 mL) to the stirred solution
  6. 6
    درجة الحرارةto reflux
  7. 7
    تركيزThe reaction was then concentrated in vacuum to a slurry
  8. 8
    workup.ADDITIONWater (200 mL) and ethyl acetate (200 mL) were added
  9. 9
    ترشيحThe reaction was then filtered through celite
  10. 10
    أخرىto remove the precipitated aluminium hydroxide
  11. 11
    أخرىthe ethyl acetate solution was separated
  12. 12
    تجفيفdried over magnesium sulfate
  13. 13
    تركيزconcentrated in vacuo

الإجراء التجريبي

2-Benzyloxy-N-(2-chloro-5-methoxy-phenyl) acetamide (2) (18.9 g, 62.0 mmol) in THF (100 mL) was stirred and lithium aluminuim hydride (4.9 g, 130.0 mmol) was added slowly over 15 min. There was a rapid evolution of hydrogen gas as the first of the lithium aluminium hydride was added. The reaction was then heated to reflux for 4 h and allowed to stand at RT over the weekend. The reaction was then quenched by the dropwise addition of water (50 mL) to the stirred solution. There was a violent evolution of hydrogen causing the reaction mixture to reflux. The reaction was then concentrated in vacuum to a slurry. Water (200 mL) and ethyl acetate (200 mL) were added and the mixture vigorously shaken. The reaction was then filtered through celite to remove the precipitated aluminium hydroxide and the ethyl acetate solution was separated, dried over magnesium sulfate and concentrated in vacuo to afford 18.4 g (quantitative) of (2-Benzyloxy-ethyl)-(2-chloro-5-methoxyphenyl) amine (3) as a gum. The structure was confirmed by 13C NMR (75 MHz, CDCl3) δC 43.3, 55.3, 68.2, 73.0, 98.1, 101.8, 111.6, 127.6, 127.7, 128.4, 129.3, 137.9, 144.8, and 159.5.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08501153B2uspto-grants-2013_08