関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2(3H)-Furanone, 3-bromodihydro- | HCID 95463 | — |
| 反応物 | Methyl 5-(benzyloxy)-2-hydroxybenzoate | HCID 13026913 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | alpha-[(2-Carboxy-4-benzyloxyphenyl)oxy]-gamma-butyrolactone | HCID 12925947 | — |
反応手順
To a mixture of 32 g of methyl 5-benzyloxysalicylate, 17 g of anhydrous potassium carbonate and 500 ml of acetone was added 30.7 g of α-bromo-γ-butyrolactone under cooling with ice and, then, the mixture was refluxed for 15 hours. After cooling, the acetone was distilled off and 10% methanolic sodium hydroxide was added to the residue for hydrolysis. The reaction mixture was made acidic with hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and distilled to remove the solvent. The residue was dissolved in dioxane (300 ml)-benzene (200 ml) and the solution was refluxed in the presence of p-toluenesulfonic acid (30 g), with the resultant water being continuously distilled off. The solvent was distilled off and the residue was diluted with water and extracted with ethyl acetate. The extract was washed with water, dried and concentrated to remove the solvent. The residue was recrystallized from ethyl acetate. By the above procedure there was obtained α-[(2-carboxy-4-benzyloxyphenyl)oxy]-γ-butyrolactone as colorless needles, m.p. 120°-122° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04284644 |
|---|
| 出典データセット | uspto-grants-1981_08 |
|---|
| ORD ID | ord-5a23af22caa248a99bb08954c267b36c |
|---|
| 出典メモ | uspto-grants-1981_08 |
|---|