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HRID 375994作成日:2026年10月24日

Methyl formate → 3-Oxo-cyclopentanecarboxylic acid methyl ester

https://huagongshe.com/ja/reaction/375994

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl formateHCID 7865—
反応物Trimethyl orthoformateHCID 9005—
反応物3-Oxocyclopentanecarboxylic acidHCID 227798—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
生成物3-Oxo-cyclopentanecarboxylic acid methyl esterHCID 237640—

反応条件

温度10 °C

反応手順

318.36 g (3 mol) of trimethylorthoformate are added gradually to a solution of 128.2 g (1 mol) of nonracemic 3-oxocyclopentanecarboxylic acid and 11.4 g (0.06 mol) of p-toluene sulfonic acid hydrate in 380 ml of methanol within 5-10 minutes while stirring, The mixture is heated and during 25 minutes a mixture of formic acid methyl ester and methanol is distilled off (about 185 g of distillate), Thereafter 29 g of 30% sodium methylate solution (0.16 mol) are added and the reaction mixture is kept boiling under reflux for 2 hours; methanol is distilled off, the residue cooled to 10° C. and dissolved by adding 230 ml of methylene chloride and 200 ml of water. By adding 5% sulfuric acid the mixture is adjusted to pH 1.4 and stirred at 10° C. for 30 minutes. The methylene chloride phase is separated and the aqueous phase extracted again with 100 ml of methylene chloride. The combined organic phases are stirred with 50 ml of water, separated and the solvent is distilled off in vacuo. The residue is fractionated in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05488136
出典データセットuspto-grants-1996_01
ORD IDord-c7e2963c623b4c9b8cea55662fcbef8f
出典メモuspto-grants-1996_01