Diethyl Ether → 2-Methyl-3-tetrahydropyranyloxypropanal

HRID 329791

反応式

HRID 329791 の反応式
[CH3:1][CH:2]([CH2:5][O:6][CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][O:8]1)[CH2:3][OH:4].[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1.CCOCC>ClCCl>[CH3:1][CH:2]([CH2:5][O:6][CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][O:8]1)[CH:3]=[O:4]

参加物

5

実験手順

A solution of 2-methyl-3-tetrahydropyranyloxy-1-propanol (250 mg; 1.4 mmol) in dichloromethane (4 ml) was added to a suspension of pyridinium chlorochromate (500 mg; 2.32 mmol) and celite (2.5 g) in dichloromethane (10 ml), and stirred at room temperature for 3 hours. Ether (100 ml) was added thereto. The resultant mixture was filtered, and the filtrate was distilled under reduced pressure to give the solvent. The residue was purified by silica gel chromatography using a mixture of ethyl acetate and benzene (1:4) to give 2-methyl-3-tetrahydropyranyloxypropanal (178 mg; yield, 73%).

後処理

  1. filtrationThe resultant mixture was filtered
  2. distillationthe filtrate was distilled under reduced pressure
  3. customto give the solvent
  4. customThe residue was purified by silica gel chromatography
  5. additiona mixture of ethyl acetate and benzene (1:4)

出典と根拠

ORDレコード
ord-d5b612101e3845bcbc1e930156c6f691
出典データセット
uspto-grants-1990_01
特許番号
US04892961

関連ノート

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