تفاعل #1605774

ord-52881c44bbf845548246dbffcb54e623

معادلة التفاعل

Cc1ccc(Br)nc1
2-bromo-5-methylpyridine
CC#N
acetonitrile
[Li][CH2]CCC
n-BuLi
Cc1ccc(CC#N)nc1
2-(5-methylpyridin-2-yl)acetonitrile

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITThe reaction mixture was kept at −78° C. for 1 hr
  2. 2
    درجة الحرارةthen warmed up slowly
  3. 3
    workup.STIRRINGstirred for another 1 hr
  4. 4
    أخرىthe layer was separated
  5. 5
    غسيلThe organic layer was washed with water and brine
  6. 6
    تجفيفdried over MgSO4
  7. 7
    ترشيحfiltered
  8. 8
    أخرىevaporated

الإجراء التجريبي

To a solution of anhydrous acetonitrile (10.1 mL, 191.83 mmol, 3.3 eq) in dry THF (500 mL) was added dropwise n-BuLi (2.5 M in Hexane, 69.8 mL, 174.39 mmol, 3 eq) at −78° C. under N2 atmosphere. The resulting white suspension was stirred at −78° C. for 1 hr, and then a solution of 2-bromo-5-methylpyridine (10.0 g, 58.13 mmol, 1 eq) in dry THF (30 mL) was added. The reaction mixture was kept at −78° C. for 1 hr then warmed up slowly to r.t and stirred for another 1 hr. Ice/water was added and the layer was separated. The organic layer was washed with water and brine, dried over MgSO4, filtered and evaporated to give 18 g of crude 2-(5-methylpyridin-2-yl)acetonitrile. Since the product is very volatile, it was not dried under high vacuum and still contains some solvent.

المصدر

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