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HRID 229727作成日:2026年10月24日

Benzoic acid, 3,5-dihydroxy-, ethyl ester → Ethyl 3-hydroxy-5-oxo-3-cyclohexene-1-carboxylate

https://huagongshe.com/ja/reaction/229727

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoic acid, 3,5-dihydroxy-, ethyl esterHCID 20098—
反応物Sodium FormateHCID 2723810—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Ethyl 3-hydroxy-5-oxo-3-cyclohexene-1-carboxylateHCID 1055937915.1%

反応手順

3,5-Dihydroxybenzoic acid ethyl ester (10 g, 54.89 mmol) was dissolved in ethanol (15 mL), followed by adding sodium formate (4.48 g, 65.87 mmol), replacing inside a reactor with nitrogen at 30° C. for 15 minutes, adding palladium on carbon (364 mg) and reacting at 30° C. for 3 hours then at 40° C. over night. Catalyst was filtered off, followed by neutralization with a 1N HCl solution, concentration under reduced pressure and purification of thus obtained residue with silica gel column chromatography (hexane/ethyl acetate=1/1 to 0/1) to obtain an objective compound (1.53 g, 15.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563893B2
出典データセットuspto-grants-2009_07
ORD IDord-1fb85f8cf26c47ed86e59354a3ca2edb
出典メモuspto-grants-2009_07