Aluminium lithium hydride → Thieno[3,2-c]pyridin-2-ylmethanol
反応式
[S:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[C:2]1[C:10](OC)=[O:11].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[S:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[C:2]1[CH2:10][OH:11]参加物
4
反応条件
- 温度
- 0 °C
実験手順
To a solution of methyl thieno[3,2-c]pyridine-2-carboxylate (D-2) (15 g, 77.6 mmol) in anhydrous THF (250 mL) was added LiAlH4 (4.42 g, 116.4 mmol) in portions at 0° C. The suspension was stirred at 0° C. for 1 h and then quenched by adding saturated aqueous NH4Cl and filtered. The filtrate was washed with brine and concentrated. The residue was used in the next step without any further purification (10.3 g).
後処理
- customquenched
- additionby adding saturated aqueous NH4Cl
- filtrationfiltered
- washThe filtrate was washed with brine
- concentrationconcentrated
- customThe residue was used in the next step without any further purification (10.3 g)
出典と根拠
- ORDレコード
- ord-6b7c4c9efd8e46a58e4caeac72e0c018
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987269B2
反応ノート
読み込み中…