Diisobutylaluminum hydride → (R)-3-(tert-butyldimethylsilyloxy)-4-chlorobutanal

HRID 530000노트

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HRID 530000 반응식
[Si:1]([O:8][C@@H:9]([CH2:15][Cl:16])[CH2:10][C:11](OC)=[O:12])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].CC(C[AlH]CC(C)C)C>CO>[Si:1]([O:8][C@@H:9]([CH2:15][Cl:16])[CH2:10][CH:11]=[O:12])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]

참가 물질

4

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온도
-78 °C

실험 절차

To a solution of (R)-methyl 3-(tert-butyldimethylsilyloxy)-4-chlorobutanoate (2.13 g, 104.7 mmol) in CH3Cl2 was added dropwise DIBAL-H (120 mL, 1 M in toluene, 120 mmol) at −78° C. under N2 atmosphere. The mixture was stirred at −78° C. for 4 h. CH3OH (80 mL) was added slowly to the reaction, mixture at −78° C. Then the temperature was warmed to room temperature gradually. The mixture was filtered and the cake was washed with CH2Cl2. The combined filtrates were concentrated under reduced pressure and purified by column chromatography (PE) to give (R)-3-(tert-butyldimethylsilyloxy)-4-chlorobutanal (13 g, 60% over 2 steps). 1H NMR (300 MHz, CDCl3) δ 9.80 (t, J=1.6 Hz, 1H), 4.35-4.42 (m, 1H), 3.53 (dd, J=11.1 Hz, 4.8 Hz, 1H), 3.46 (dd, J=12 Hz, 6.3 Hz, 1H), 2.63-2.82 (m, 2H), 0.87 (s, 9H), 0.12 (s, 3H), 0.08 (s, 3H).

후처리

  1. temperatureThen the temperature was warmed to room temperature gradually
  2. filtrationThe mixture was filtered
  3. washthe cake was washed with CH2Cl2
  4. concentrationThe combined filtrates were concentrated under reduced pressure
  5. custompurified by column chromatography (PE)

출처 및 근거

ORD 기록
ord-860942903d624df8a4a268fcbe211962
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09351962B2

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