戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 54993作成日:2026年10月23日

Iodine → 4-(2-Methylbenzoyl)pyridine

https://huagongshe.com/ja/reaction/54993

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物2-BromotolueneHCID 7236—
反応物4-CyanopyridineHCID 7506—
反応物TetrahydrofuranHCID 8028—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物4-(2-Methylbenzoyl)pyridineHCID 19957162—

反応手順

To a warmed mixture of ether (500 mL) and magnesium turnings (14.9 g, 0.614 mol) was added dropwise 2-bromotoluene (105 g, 0.614 mol) and then a crystal of iodine. The reaction mixture was refluxed for 1 hour, then 4-cyanopyridine (30.2 g, 0.29 mol) in THF (130 mL) was added dropwise over 45 minutes. The mixture was refluxed for 1.5 hours, cooled to room temperature and quenched with 6N HCl (200 mL). The organic phase was separated, the aqueous phase was extracted with Et2O, and the combined ether phases were extracted with 2N HCl. The aqueous acidic phases were combined, basified with concentrated NH4OH, extracted with Et2O (3×750 mL) and the combined organic layers were dried over Na2SO4 and the solvent was removed in vacuo to afford 54 g of crude 2-isonicotinoyltoluene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624922
出典データセットuspto-grants-1997_04
ORD IDord-b9c36476f8004ffbbff6548013a1af0c
出典メモuspto-grants-1997_04