反応式
C([O:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][O:13]C(=O)C)=[CH:8][N:7]=1)(=O)C.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[H-]>O1CCCC1>[OH:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][OH:13])=[CH:8][N:7]=1参加物
6
実験手順
2,5-Di(acetoxymethyl)pyridine (0.05 mole) is reduced with lithium aluminum hydride (0.025 mole) in tetrahydrofuran (50 ml.) at 0° C. with stirring. After one hour, water is added to decompose excess hydride, and the mixture is concentrated to dryness. The residue is extracted with hot isopropanol (2×60 ml.) and the extract is concentrated to dryness to give 2,5-di(hydroxymethyl) pyridine.
後処理
- concentrationthe mixture is concentrated to dryness
- extractionThe residue is extracted with hot isopropanol (2×60 ml.)
- concentrationthe extract is concentrated to dryness
出典と根拠
- ORDレコード
- ord-6c5e1a5b524b4b2f99b7ec93b2f076ea
- 出典データセット
- uspto-grants-1985_10
- 特許番号
- US04546106
関連ノート
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