Hexane → HCID 54390831, 화합물

HRID 1379368노트

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HRID 1379368 반응식
[CH3:1][CH:2]([CH:4]1[CH2:8][O:7][C:6](=[O:9])[NH:5]1)[CH3:3].C([Li])CCC.CCCCCC.[CH3:21][CH:22]([CH3:28])[CH2:23][CH2:24][C:25](Cl)=[O:26]>O1CCCC1>[CH3:21][CH:22]([CH3:28])[CH2:23][CH2:24][C:25]([N:5]1[C@@H:4]([CH:2]([CH3:3])[CH3:1])[CH2:8][O:7][C:6]1=[O:9])=[O:26]

참가 물질

6

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온도
-78 °C

실험 절차

To a stirred solution of 4-(2-propyl)-oxazolidine-2-one in anhydrous tetrahydrofuran (250 ml) under a nitrogen atmosphere at -78° C. was added in a dropwise fashion a solution of n-butyllithium in hexane (50 ml, 77.4 mmol) over 5 to 10 min. After stirring an additional 20 min at -78° C., 4-methylpentanoyl chloride (85.2 mmol) was added neat. The reaction was warmed to room temperature and stirred 1 to 2 h at the temperature. The reaction was quenched by adding 100 ml of saturated aqueous ammonium chloride and the volatiles were removed by rotary evaporation. The resulting aqueous residue was extracted three times with ether and the combined organic phases were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. Recrystallization from hexanes/ethyl acetate provided the desired compound.

후처리

  1. temperatureThe reaction was warmed to room temperature
  2. stirringstirred 1 to 2 h at the temperature
  3. customThe reaction was quenched
  4. additionby adding 100 ml of saturated aqueous ammonium chloride
  5. customthe volatiles were removed by rotary evaporation
  6. extractionThe resulting aqueous residue was extracted three times with ether
  7. washthe combined organic phases were washed with brine
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customRecrystallization from hexanes/ethyl acetate

출처 및 근거

ORD 기록
ord-792c01d2e9904368888086ef73b63385
출처 데이터셋
uspto-grants-1997_09
특허 번호
US05670675

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