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HRID 51268作成日:2026年10月25日

4-(2,3-Dimethoxybenzoyl)pyridine → (2,3-Dimethoxyphenyl)(piperidin-4-yl)methanol

https://huagongshe.com/reaction/51268

反応式

関与物質

役割名称HCID仕込み量
反応物4-(2,3-Dimethoxybenzoyl)pyridineHCID 428549—
溶媒MethanolHCID 887—
生成物(2,3-Dimethoxyphenyl)(piperidin-4-yl)methanolHCID 1089036292.5%

反応手順

A solution of 4-(2,3-dimethoxybenzoyl)pyridine (12) (2.10 g, 8.6 mmol) in MeOH (10 mL) is treated with 5% Rh/alumina (0.72 g). The mixture is hydrogenated in a Parr shaker at 55 psig for 22 hours. After filtration through Celite7 filter aid, the filtrate is concentrated at reduced pressure to give the title compound (11) as a solid (2.0 g, 92% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713627B2
出典データセットuspto-grants-2004_03
ORD IDord-7e3f5ba32de04fa7ba8b4f049ccb6fe2
出典メモuspto-grants-2004_03