돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 703655생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/703655

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 4-chloroacetoacetateHCID 69484—
반응물2-(2-(2-Hydroxyethoxy)ethyl)-1H-isoindole-1,3(2H)-dioneHCID 2755406—
용매TetrahydrofuranHCID 8028—
생성물10-Phthalimido-3-oxo-5,8-dioxadecanoic acid ethyl esterHCID 14126617—

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04983740
출처 데이터셋uspto-grants-1991_01
ORD IDord-245dfa84df4e493ca754d84d4cd1006a
출처 메모uspto-grants-1991_01