反応式
[CH2:1]([O:3][C:4](=[O:12])[C:5]1[CH:10]=[CH:9][CH:8]=[N:7][C:6]=1[CH3:11])[CH3:2].[Se](=O)=[O:14]>O1CCOCC1>[CH2:1]([O:3][C:4](=[O:12])[C:5]1[CH:10]=[CH:9][CH:8]=[N:7][C:6]=1[CH:11]=[O:14])[CH3:2]参加物
4
実験手順
A mixture of 11.3 g (0.069 mol) of 2-methyl-nicotinic acid ethyl ester and 8.4 g (0.076 mol) of selenium dioxide in 150 mL of dioxane is refluxed under nitrogen for 4 hours. The reaction mixture is cooled to room temperature and filtered. The filtrate is evaporated and the residue is chromatographed on 400 grams of silica gel using 50/50 ethyl acetate/hexanes as the eluant. Appropriate fractions are combined to yield 5 g of 2-formyl-nicotinic acid ethyl ester. 1H NMR (CDCl3) δ 10.3 (s, 1H), 8.8 (m, 1H), 8.0 (m, 1H), 7.5 (m, 1H), 4.30 (q, 2H), 1.4 (t, 3H). TLC (7/3 hexanes/ethyl acetate) Rf=0.2. Step 2:
後処理
- temperatureis refluxed under nitrogen for 4 hours
- filtrationfiltered
- customThe filtrate is evaporated
- customthe residue is chromatographed on 400 grams of silica gel using 50/50 ethyl acetate/hexanes as the eluant
出典と根拠
- ORDレコード
- ord-2fed7c86b2fa4d0f8752b4cfc0e491bd
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06949562B2
関連ノート
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