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
- filtrationThe resultant mixture was filtered
- distillationthe filtrate was distilled under reduced pressure
- customto give the solvent
- customThe residue was purified by silica gel chromatography
- 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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