反応式
[CH3:1][C:2]1[CH:7]=[C:6](B2OC(C)(C)C(C)(C)O2)[CH:5]=[CH:4][N:3]=1.Cl[C:18]1[C:25]([CH3:26])=[CH:24][C:21]([CH:22]=[O:23])=[CH:20][N:19]=1.C(Cl)Cl.C([O-])([O-])=O.[K+].[K+].C(OC(C)C)(=O)C>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].O>[CH3:1][C:2]1[CH:7]=[C:6]([C:18]2[C:25]([CH3:26])=[CH:24][C:21]([CH:22]=[O:23])=[CH:20][N:19]=2)[CH:5]=[CH:4][N:3]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 75 °C
実験手順
To a 5-L four-necked flask equipped with an overhead stirrer, a thermocouple and a condenser was charged with 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (34b, 1120 mmol), 6-chloro-5-methylnicotinaldehyde (34c, 174.3 g, 1120 mmol), Pd(dppf)Cl2.CH2Cl2 (4.57 g, 5.6 mmol), K2CO3 (309.6 g, 2240 mmol), and iso-propyl acetate (1120 mL)/water (1120 mL). The mixture was stirred at 75° C. for 4 h, and cooled to 30° C. The organic layer was separated, washed with 10% NaCl (1120 g), and treated with activated charcoal (50 g) at 50° C. for 2 h before cooling to rt and filtered through Celite. Concentration of the filtrate to almost dryness afforded the crude 2′,3-dimethyl-[2,4′-bipyridine]-5-carbaldehyde (34d) as a brown oil.
後処理
- customTo a 5-L four-necked flask equipped with an overhead stirrer
- temperaturecooled to 30° C
- customThe organic layer was separated
- washwashed with 10% NaCl (1120 g)
- additiontreated with activated charcoal (50 g) at 50° C. for 2 h
- temperaturebefore cooling to rt
- filtrationfiltered through Celite
出典と根拠
- ORDレコード
- ord-a36e2845d6c54bea82f284b44f18b16b
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09181235B2
関連ノート
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