تفاعل #1973908
ord-a6dc42d530284376b579ab4a6f704085
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwas added
- 2درجة الحرارةThe reaction was then heated
- 3درجة الحرارةto reflux for 4 h
- 4أخرىto stand at RT over the weekend
- 5أخرىThe reaction was then quenched by the dropwise addition of water (50 mL) to the stirred solution
- 6درجة الحرارةto reflux
- 7تركيزThe reaction was then concentrated in vacuum to a slurry
- 8workup.ADDITIONWater (200 mL) and ethyl acetate (200 mL) were added
- 9ترشيحThe reaction was then filtered through celite
- 10أخرىto remove the precipitated aluminium hydroxide
- 11أخرىthe ethyl acetate solution was separated
- 12تجفيفdried over magnesium sulfate
- 13تركيزconcentrated 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.