戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 37357作成日:2026年10月25日

Methanol → Methyl 6-bromopyridine-3-carboxylate

https://huagongshe.com/reaction/37357

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物DibromomethaneHCID 3024—
反応物HCID 178418479HCID 178418479—
生成物Methyl 6-bromopyridine-3-carboxylateHCID 13349623—

反応条件

温度70 °C

反応手順

6-Hydroxynicotinic acid (31 g) and methylene bromide (300 mL) were added at 18° C. to 98.9 g of phosphorous pentabromide while stirring with a mechanical stirrer under an argon atmosphere. The mixture was warmed to 70° C. over 2 hours, and further stirred for 16 hours. The mixture was cooled to 10° C. and 300 mL of methanol (CAUTION: EXOTHERMIC) was added. The cooling bath was removed and stirring was continued for 1/2 hour more. A solution of 76 g of K2CO3 in 610 mL of water was added and stirred for a few minutes. The layers were separated. The aqueous layer was extracted with methylene bromide. The combined organic phase was filtered through celite, washed with water and stripped. The residue was dissolved in 200 mL of ethanol on the steam bath. To this hot solution, 400 mL of water was added and the mixture was cooled in an ice bath. The precipitated solid was filtered, washed with 20% ethanol in water and air-dried to give 38.3 g of methyl 6-bromo-nicotinate as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420270
出典データセットuspto-grants-1995_05
ORD IDord-d508abd3dae2446abb3e294f93225b27
出典メモuspto-grants-1995_05