Methanol → (R)-3-(tert-butyldimethylsilyloxy)-4-chlorobutanal

HRID 1673131노트

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HRID 1673131 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>C(Cl)Cl>[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

5

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온도
-78 °C

실험 절차

To a solution of (R)-methyl 3-(tert-butyldimethylsilyloxy)-4-chlorobutanoate (27.9 g, 104.7 mmol) in CH2Cl2 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) δ9.80 (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-5b52781ed471400fa5d624d53a6e1a8f
출처 데이터셋
uspto-grants-2011_08
특허 번호
US07999113B2

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