Methyl iodide → 3,3-Dimethyl-tetrahydro-pyran-2-one

HRID 979530노트

반응식

HRID 979530 반응식
[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][O:4][C:3]1=[O:8].[Li+].[CH3:10]C([N-]C(C)C)C.CC(C)=O.C(=O)=O.CI>C1COCC1>[CH3:1][C:2]1([CH3:10])[CH2:7][CH2:6][CH2:5][O:4][C:3]1=[O:8]

참가 물질

6

반응 조건

온도
-45 °C

실험 절차

The 3-methyltetrahydro-2H-pyran-2-one from Example 4(a) (5.6 g, 49.0 mmol) was slowly added to a cold (-78° C.) THF solution (50 ml) of LDA (54 mmol) so that the internal temperature did not exceed -65° C. After stirring for an additional 30 minutes, the acetone/CO2 bath was replaced with a CH3CN/CO2 bath and CH3I (10.4 g, 73.5 mmol) was added at a rate sufficient to maintain the internal temperature at -45° C. After stirring at -45° C. for an additional hour the reaction was allowed to warm to -30° C. and quenched by the dropwise addition of 10% HCl (21 ml). The resulting mixture was poured into ether (300 ml) and the ether layer was washed with saturated brine (50 ml), saturated NaHCO3 solution (20 ml), saturated brine (2×25 ml), dried (MgSO4) and evaporated to provide a pale yellow oil. This oil was distilled to give the title compound as a colorless liquid. b.p.0.2 54° C. NMR (CDCl3) δ4.34 (2H, m), 1.89 (2H, m), 1.75 (2H, m), 1.30 (6H, s).

후처리

  1. customdid not exceed -65° C
  2. stirringAfter stirring at -45° C. for an additional hour the reaction
  3. temperatureto warm to -30° C.
  4. customquenched by the dropwise addition of 10% HCl (21 ml)
  5. additionThe resulting mixture was poured into ether (300 ml)
  6. washthe ether layer was washed with saturated brine (50 ml), saturated NaHCO3 solution (20 ml), saturated brine (2×25 ml)
  7. dry with materialdried (MgSO4)
  8. customevaporated
  9. customto provide a pale yellow oil
  10. distillationThis oil was distilled

출처 및 근거

ORD 기록
ord-c24c0e8973dd43be98af57f4b306e8d2
출처 데이터셋
uspto-grants-1987_05
특허 번호
US04668699

반응 노트

불러오는 중…