반응 #55318

ord-c848ad90b5f249fcaa1746e449176934

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도While maintaining the reaction mixture at 5°-10° C.
  2. 2
    workup.ADDITIONthe addition
  3. 3
    온도the reaction mixture was warmed to 35°
  4. 4
    온도maintained for 15 mins at this temperature
  5. 5
    온도The reaction was then cooled to 15°-20°
  6. 6
    기타carefully quenched by dropwise addition of water
  7. 7
    추출extracted with ether
  8. 8
    건조The combined ether extracts were dried over anhydrous magnesium sulfate
  9. 9
    여과filtered
  10. 10
    농축concentrated under reduced pressure
  11. 11
    기타to give 45 g crude product
  12. 12
    workup.DISTILLATIONDistillation

실험 절차

While maintaining the reaction mixture at 5°-10° C., 3-pyridylcarbinol (50.0 g., 0.45 mol) was slowly added to a mixture of sodium hydride (24.0 g of a 50% suspension in mineral oil, 0.5 mol) in 250 ml dry N,N-dimethylformamide. Propargyl chloride (37.0 g, 0.5 mole) was then slowly added to this mixture at 15° C. Following the addition, the reaction mixture was warmed to 35° and maintained for 15 mins at this temperature. The reaction was then cooled to 15°-20°, carefully quenched by dropwise addition of water and extracted with ether. The combined ether extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 45 g crude product. Distillation gave 30.0 g of 3-(2-propynyloxymethyl)pyridine. Yield 44% theory; b.p. 95° C. (0.9 mm).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04220577uspto-grants-1980_09