反応式
[BH4-].[Na+].[N:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[C:5](C=O)[CH:4]=1.[CH3:15][OH:16]>>[N:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[CH2:15][OH:16])[CH:6]=[CH:5][CH:4]=1参加物
4
実験手順
Sodium borohydride (280 mg, 7.4 mmol) was added in portions to a solution of 3-quinoline-carboxaldehyde (1.06 g, 6.7 mmol) in methanol at room temperature. Reaction was quenched after 3 hours stirring with 10 mL (aq) sat. NH4Cl. Mixture was extracted with ethyl acetate (3×30 ml). Combined organics were washed with brine and dried over MgSO4. Crude material was purified by chromatography using (20-40% EA/Hex gradient) to afford quinolin-8-yl-methanol as an off white solid (800 mg; 75% yield).
後処理
- customReaction
- customwas quenched after 3 hours
- extractionMixture was extracted with ethyl acetate (3×30 ml)
- washCombined organics were washed with brine
- dry with materialdried over MgSO4
- customCrude material was purified by chromatography
出典と根拠
- ORDレコード
- ord-a0a5b2fa8a214858bb604d761aeba86c
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07888366B2
関連ノート
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