Diisobutylaluminum hydride → HCID 59278372、化合物
反応式
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([CH3:10])[N:7]=[C:6]([Br:11])[CH:5]=1.CC(C[AlH]CC(C)C)C>C(Cl)Cl>[Br:11][C:6]1[CH:5]=[C:4]([CH2:3][OH:2])[CH:9]=[C:8]([CH3:10])[N:7]=1参加物
実験手順
To a chilled (−78° C.) solution of 2-bromo-6-methyl-isonicotinic acid methyl ester (1.90 g, 8.26 mmol) in CH2Cl2 (200 mL) was added a 1 M solution of DIBAH (24.8 mL, 24.8 mmol) in CH2Cl2. The mixture was allowed to warm to room temperature. After 12 hours, the reaction was quenched with saturated aqueous sodium bicarbonate (100 mL). After 5 hours, phases were separated and the aqueous layer was extracted with CH2Cl2 (3×100 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4, filtered and concentrated. The resulting residue was purified by silica gel chromatography eluting with a gradient of 0-100% ethyl acetate in heptane to afford (2-bromo-6-methyl-pyridin-4-yl)-methanol as white solid. MS m/z 202.45 (M+), 204.44 (M+2).
後処理
- customthe reaction was quenched with saturated aqueous sodium bicarbonate (100 mL)
- waitAfter 5 hours
- customphases were separated
- extractionthe aqueous layer was extracted with CH2Cl2 (3×100 mL)
- washThe combined organic layers were washed with brine (100 mL)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe resulting residue was purified by silica gel chromatography
- washeluting with a gradient of 0-100% ethyl acetate in heptane
出典と根拠
- ORDレコード
- ord-a0b5141d04b44b1c97a9024326bd67e4
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07879873B2
反応ノート
読み込み中…