Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358301생성일: 2026년 10월 25일
Triphenylphosphine → Benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl ester
https://huagongshe.com/reaction/358301
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 2,4-Dimethoxybenzyl alcohol | HCID 81750 | — |
| 반응물 | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| 반응물 | Benzyloxycarbonyl-2-(2,5-dioxopyrrolidin-3-yl)glycine methyl ester | HCID 13105389 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04465844 |
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| 출처 데이터셋 | uspto-grants-1984_08 |
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| ORD ID | ord-7f80ed19ce8148eea873befe7a1827be |
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| 출처 메모 | uspto-grants-1984_08 |
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