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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358301생성일: 2026년 10월 24일

Triphenylphosphine → Benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl ester

https://huagongshe.com/ko/reaction/358301

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2,4-Dimethoxybenzyl alcoholHCID 81750—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물Benzyloxycarbonyl-2-(2,5-dioxopyrrolidin-3-yl)glycine methyl esterHCID 13105389—
용매TetrahydrofuranHCID 8028—
생성물Benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl esterHCID 20449787—

반응 단계

In 100 ml of tetrahydrofuran were dissolved 3.2 g of benzyloxycarbonyl-2-(2,5-dioxopyrrolidin-3-yl)glycine methyl ester, 1.8 g of 2,4-dimethoxybenzyl alcohol and 3.9 g of triphenylphosphine and under ice-cooling 2 ml of diethyl azodicarboxylate was added. The mixture was stirred at room temperature for one hour and concentrated under reduced pressure. The residue was dissolved in ethyl acetate, and the solution was washed with 5% sodium hydrogen carbonate and 10% phosphoric acid in that order and dried over sodium sulfate. The solution was concentrated under reduced pressure and the concentrate was chromatographed on a silica gel column, elution being carried out with toluene-ethyl acetate (7:3). The eluate was concentrated under reduced pressure and to the residue was added petroleum ether. The precipitate was collected by filtration and dried. Yield 1.2 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04465844
출처 데이터셋uspto-grants-1984_08
ORD IDord-7f80ed19ce8148eea873befe7a1827be
출처 메모uspto-grants-1984_08