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HRID 894610作成日:2026年10月26日

Potassium Carbonate → alpha-[(2-Carboxy-4-benzyloxyphenyl)oxy]-gamma-butyrolactone

https://huagongshe.com/reaction/894610

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2(3H)-Furanone, 3-bromodihydro-HCID 95463—
反応物Methyl 5-(benzyloxy)-2-hydroxybenzoateHCID 13026913—
溶媒AcetoneHCID 180—
生成物alpha-[(2-Carboxy-4-benzyloxyphenyl)oxy]-gamma-butyrolactoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04284644
出典データセットuspto-grants-1981_08
ORD IDord-5a23af22caa248a99bb08954c267b36c
出典メモuspto-grants-1981_08