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Methanol → (2S)-2-(Benzyloxy)propanal

HRID 278466
ノート
印刷プレビュー

反応式

HRID 278466 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

HCID 11116387(2S)-2-(Benzyloxy)propanal収率 49.4%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒
HCID 8058
Hexane
溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-a299659aa09441b792451ee49187a30d
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06359145B1

反応ノート

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