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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 653694생성일: 2026년 10월 26일

Triethylamine → N-(2,3-dimethylnaphthyl)-N-(2-oxo-tetrahydrofuran-3-yl)-N-(2-methoxy-ethoxy-acetyl)-amine

https://huagongshe.com/reaction/653694

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(2-Methoxyethoxy)acetyl chlorideHCID 7010338—
반응물N-(2,3-dimethylnaphtyl)-N-(2-oxo-tetrahydrofuran-3-yl)-amineHCID 13092367—
용매TolueneHCID 1140—
생성물N-(2,3-dimethylnaphthyl)-N-(2-oxo-tetrahydrofuran-3-yl)-N-(2-methoxy-ethoxy-acetyl)-amineHCID 67917313—

반응 단계

To 15.3 g of N-(2,3-dimethylnaphtyl)-N-(2-oxo-tetrahydrofuran-3-yl)-amine in 120 ml of toluene are added dropwise 12.2 g of 2-methoxyethoxy-acetyl chloride (MAC) in 20 ml of toluene and afterwards 8.1 g of triethylamine in 20 ml of toluene. The temperature of the reaction rises to 35° and is then raised to 40° for 2 hours. There are subsequently added dropwise a further 2 g of MAC and 1.5 g of triethylamine. The temperature is held overnight at 40°, and afterwards a further 2 g of MAC are added dropwise. After 4 hours, the reaction mixture is cooled to room temperature and filtered, and the filtrate is concentrated by evaporation to yield a resinous residue, which is purified through silica gel 60 using ethyl acetate as the eluant. The solid product occurring from the residue is recrystallised from isopropanol with the addition of active charcoal. The resulting product is the colourless diastereoisomeric mixture of the compound No. 32, m.p. 142°-146°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05128371
출처 데이터셋uspto-grants-1992_07
ORD IDord-c433676cfe3a49bcbd1730250bdf12da
출처 메모uspto-grants-1992_07