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Methanol → (2S)-2-(Benzyloxy)propanal

HRID 278466
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HRID 278466 반응식
[H-].C([Al+]CC(C)C)C(C)C.[CH2:11]([O:18][C@@H:19]([CH3:25])[C:20](OCC)=[O:21])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(=O)=O.CC(C)=O.CO>CCCCCC.C(Cl)Cl>[CH2:11]([O:18][C@@H:19]([CH3:25])[CH:20]=[O:21])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 887MethanolHCID 10058881Ethyl (2S)-2-(benzyloxy)propanoateHCID 18522661Acetone cardiceHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 11116387(2S)-2-(Benzyloxy)propanal수율 49.4%

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 8058Hexane용매

실험 절차

A solution of 1.0M DIBAL (diisobutylaluminum hydride) in hexane (10 ml) was added dropwise to a stirred solution of ethyl (S)-2-(benzyloxy)propionate (obtained in Preparation 7) (2.08 g) in methylene chloride (20 ml) at −78° C. (dry-ice/acetone) for 5 minutes under nitrogen atmosphere. After 20 minutes, methanol (1.6 ml) was added dropwise to the mixture at −78° C., and the resulting mixture was stirred at room temperature for 30 minutes. The mixture was filtered through a pad of Celite, and the solid on the filter was washed with methylene chloride. The combined filtrates were concentrated in vacuo. The obtained residue was purified by silica gel (35 g) chromatography eluted with hexane/ethyl acetate (30:1) to give (S)-2-(benzyloxy)propionaldehyde (810 mg).

후처리

  1. filtrationThe mixture was filtered through a pad of Celite
  2. washthe solid on the filter was washed with methylene chloride
  3. concentrationThe combined filtrates were concentrated in vacuo
  4. customThe obtained residue was purified by silica gel (35 g) chromatography
  5. washeluted with hexane/ethyl acetate (30:1)

출처 및 근거

ORD 기록
ord-a299659aa09441b792451ee49187a30d
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06359145B1

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