Methanol → Methyl 2-(5-bromopyridin-3-yl)acetate
反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([OH:11])=[O:10])[CH:5]=[N:6][CH:7]=1.S(Cl)(Cl)=O.[CH3:16]O>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][C:9]([O:11][CH3:16])=[O:10])[CH:5]=[N:6][CH:7]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
To a suspension of 2-(5-bromopyridin-3-yl)acetic acid (5 g, 23.14 mmol) in MeOH (100 mL) was added thionyl chloride (1.858 mL, 25.5 mmol) at 0° C., and the mixture was stirred at 0° C. for 2 h. The mixture was concentrated in vacuo, re-dissolved in DCM (100 mL) and MeOH (10 mL), and saturated NaHCO3 in water (5 mL) was added, followed with NaHCO3 (10 g). To the mixture was added silica gel (10 g) and the mixture was concentrated. The residue was purified by silica chromatography eluting with 0-50% EtOAc-heptane to give methyl 2-(5-bromopyridin-3-yl)acetate. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.64 (s, 3H), 3.80 (s, 2H), 8.01 (dd, J=2.0 Hz, 1H), 8.48 (d, J=1.8 Hz, 1H), 8.61 (d, J=2.3 Hz, 1H).
後処理
- concentrationThe mixture was concentrated in vacuo
- dissolutionre-dissolved in DCM (100 mL)
- additionMeOH (10 mL), and saturated NaHCO3 in water (5 mL) was added
- additionTo the mixture was added silica gel (10 g)
- concentrationthe mixture was concentrated
- customThe residue was purified by silica chromatography
- washeluting with 0-50% EtOAc-heptane
出典と根拠
- ORDレコード
- ord-7ca55e2e02b34bd78f2b6521da4abef5
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08383827B2
反応ノート
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