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Benzoic acid, 3,5-dihydroxy-, ethyl ester → Ethyl 3-hydroxy-5-oxo-3-cyclohexene-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzoic acid, 3,5-dihydroxy-, ethyl ester | HCID 20098 | — |
| 反応物 | Sodium Formate | HCID 2723810 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Ethyl 3-hydroxy-5-oxo-3-cyclohexene-1-carboxylate | HCID 10559379 | 15.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07563893B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-1fb85f8cf26c47ed86e59354a3ca2edb |
| 出典メモ | uspto-grants-2009_07 |