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HRID 385855作成日:2026年10月27日

Methanol → 2-(6-Bromopyridin-2-yl)acetic acid

https://huagongshe.com/reaction/385855

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium HydroxideHCID 14798—
反応物2-(6-Bromopyridin-2-yl)acetonitrileHCID 642864—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-(6-Bromopyridin-2-yl)acetic acidHCID 46835714—

反応条件

温度80 °C

反応手順

(6-Bromopyridin-2-yl)acetonitrile (50 mg, 0.25 mmol) was taken up in methanol (2 mL) and 1 N aqueous sodium hydroxide (2 ml, 2 mmol) was added. The reaction was heated to 80° C. overnight. Upon completion, the reaction was cooled to ambient temperature, diluted with ethyl acetate (15 mL) and water (15 mL), and the layers were separated. The aqueous layer was acidified with 2N aqueous hydrochloric acid and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo to afford the title compound which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367706B2
出典データセットuspto-grants-2013_02
ORD IDord-aeefa89cac284b3c991110c380b5d1c7
出典メモuspto-grants-2013_02