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HRID 703655作成日:2026年10月26日

Hydrochloric Acid → 10-Phthalimido-3-oxo-5,8-dioxadecanoic acid ethyl ester

https://huagongshe.com/reaction/703655

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 4-chloroacetoacetateHCID 69484—
反応物2-(2-(2-Hydroxyethoxy)ethyl)-1H-isoindole-1,3(2H)-dioneHCID 2755406—
溶媒TetrahydrofuranHCID 8028—
生成物10-Phthalimido-3-oxo-5,8-dioxadecanoic acid ethyl esterHCID 14126617—

反応条件

温度25 °C

反応手順

77 g of 2-[2-(phthalimido)ethoxy]ethanol are added, in portions, to a suspension of 31 g of sodium hydride in 400 ml of tetrahydrofuran, while maintaining the temperature in the vicinity of 25° C. The mixture is stirred for one hour and 53.6 g of ethyl chloroacetoacetate are then added, while maintaining the temperature of the mixture at -20° C. The mixture is allowed to stand overnight at ambient temperature and then hydrolyzed with 1 l of 1N hydrochloric acid. Decantation, followed by extraction with ether are carried out and the organic phases are combined. The combined organic phase is washed with water and then dried over magnesium sulfate. It is concentrated and the residue thereby obtained (110 g) is purified by silica column chromatography using a dichloromethane:acetone (95:5) mixture as the eluting solvent. After removing the eluting solvent, 35.7 g of 10-phthalimido-3-oxo-5,8-dioxadecanoic acid ethyl ester are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04983740
出典データセットuspto-grants-1991_01
ORD IDord-245dfa84df4e493ca754d84d4cd1006a
出典メモuspto-grants-1991_01