تفاعل #992745

معادلة التفاعل

(±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl

Potassium tert-butoxide

morpholine

4-bromo-2,6-dimethylaniline

→

title compound

المردود 41.0%

2,6-Dimethyl-4-morpholin-4-yl-phenylamine

المردود 41.0%

المذيبات

toluene

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةThe reaction mixture was heated
2. 2
   درجة الحرارةto reflux for 16 hours under argon
3. 3
   درجة الحرارةcooled
4. 4
   ترشيحfiltered through silica (200 g)
5. 5
   workup.ADDITIONBrine (250 mL) was added
6. 6
   استخلاصthe mixture was extracted with ethyl acetate (3×200 mL)
7. 7
   تجفيفThe combined organic phases were dried over magnesium sulfate
8. 8
   تركيزconcentrated in vacuo
9. 9
   workup.DISSOLUTIONThe crude product was dissolved in diethyl ether (250 mL)
10. 10
    ترشيحfiltered through silica (200 g)
11. 11
    تركيزconcentrated in vacuo

الإجراء التجريبي

Bis(dibenzylideneacetone)palladium (2.88 g) and (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (4.69 g) were added to dry toluene (175 mL purged with argon) and stirred for 15 minutes under argon. Potassium tert-butoxide (7.06 g), morpholine (8.7 mL) and 4-bromo-2,6-dimethylaniline (10.03 g) were added subsequently. The reaction mixture was heated to reflux for 16 hours under argon, cooled and filtered through silica (200 g). Brine (250 mL) was added and the mixture was extracted with ethyl acetate (3×200 mL). The combined organic phases were dried over magnesium sulfate and concentrated in vacuo. The crude product was dissolved in diethyl ether (250 mL), filtered through silica (200 g) and concentrated in vacuo to furnish 8.5 g (41% yield) of the title compound as a dark oil. The product was used without further purification. GC-MS (m/z) 206 (M+); tR=6.90. 1H NMR (500 MHz, CDCl3): 2.18 (s, 6H), 3.02 (m, 4H), 3.85 (m, 4H), 6.62 (b, 2H).

المصدر