Methyl iodide → Diisopropyl (2R,3S)-2-hydroxy-3-methylsuccinate

HRID 888205노트

반응식

HRID 888205 반응식
[CH:1]([O:4][C:5](=[O:15])[C@H:6]([CH2:8][C:9]([O:11][CH:12]([CH3:14])[CH3:13])=[O:10])[OH:7])([CH3:3])[CH3:2].[CH3:16][Si]([N-][Si](C)(C)C)(C)C.[Li+].IC.[NH4+].[Cl-]>C1COCC1.O>[CH3:16][C@@H:8]([C@@H:6]([OH:7])[C:5]([O:4][CH:1]([CH3:2])[CH3:3])=[O:15])[C:9]([O:11][CH:12]([CH3:14])[CH3:13])=[O:10]

참가 물질

7

반응 조건

온도
20 °C

실험 절차

To a cold (−78° C.) solution of diisopropyl-(S)-(−)-malate (4.72 mL, 22.9 mmol, 1 eq.) in anhydrous THF (8.50 mL) was added slowly a solution (1 M) of lithium bis(trimethylsilyl)amide (48.1 mL, 48.1 mmol, 2.10 eq.) in THF. The temperature was raised to 20° C. over 30 minutes, than lowered again to −78° C. Iodomethane (1.7 mL, 28 mmol, 1.20 eq.) was added and the mixture stirred at RT for 16 hours. The reaction mixture was then cooled to 0° C. and a saturated solution of NH4Cl was added. The resulting mixture was diluted with water, extracted three times with EtOAc. The combined organic phases were washed with brine, dried over MgSO4, filtered and evaporated under reduced pressure. The residue was then purified by chromatography (SiO2, 20/80 EtOAc/c-hex) to give the product (mixture of diatereoisomers) as a colourless oil (3.77 g, 71%).

후처리

  1. customthan lowered again to −78° C
  2. temperatureThe reaction mixture was then cooled to 0° C.
  3. extractionextracted three times with EtOAc
  4. washThe combined organic phases were washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated under reduced pressure
  8. customThe residue was then purified by chromatography (SiO2, 20/80 EtOAc/c-hex)
  9. customto give

출처 및 근거

ORD 기록
ord-74e584a170694903a647c786b6e3f8b4
출처 데이터셋
uspto-grants-2012_08
특허 번호
US08247437B2

반응 노트

불러오는 중…