تفاعل #1605775

ord-4184a2ab89c04c4d956d997123143e0a

معادلة التفاعل

O
water
Cl
HCl
Cc1ccc(CC#N)nc1
2-(5-methylpyridin-2-yl)acetonitrile
B.C1CCOC1
Borane tetrahydrofuran
Cc1ccc(CCN)nc1
2-(5-methylpyridin-2-yl)ethanamine
المردود 41.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction was cooled to room temperature
  2. 2
    درجة الحرارةthe reaction mixture was then heated at 70° C. for 2 hrs
  3. 3
    درجة الحرارةAfter cooling
  4. 4
    غسيلthe resulting solution was washed with ether
  5. 5
    أخرىwas basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3
  6. 6
    استخلاصthen extracted with ether (5×100 mL)
  7. 7
    تجفيفThe organic layer was dried over MgSO4
  8. 8
    ترشيحfiltered
  9. 9
    أخرىevaporated

الإجراء التجريبي

To a solution of 18 g of crude 2-(5-methylpyridin-2-yl)acetonitrile in dry THF (100 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 232 mL, 232.5 mmol, 4 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq.HCl (6 N, 40 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ether (5×100 mL). The organic layer was dried over MgSO4, filtered and evaporated to give 7.6 g of crude 2-(5-methylpyridin-2-yl)ethanamine. (96% crude yield)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09072313B2uspto-grants-2015_07