반응 #1605774

ord-52881c44bbf845548246dbffcb54e623

반응 방정식

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

용매

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITThe reaction mixture was kept at −78° C. for 1 hr
  2. 2
    온도then warmed up slowly
  3. 3
    workup.STIRRINGstirred for another 1 hr
  4. 4
    기타the layer was separated
  5. 5
    세척The organic layer was washed with water and brine
  6. 6
    건조dried over MgSO4
  7. 7
    여과filtered
  8. 8
    기타evaporated

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09072313B2uspto-grants-2015_07