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HRID 358301作成日:2026年10月25日

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

https://huagongshe.com/reaction/358301

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物2,4-Dimethoxybenzyl alcoholHCID 81750—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物Benzyloxycarbonyl-2-(2,5-dioxopyrrolidin-3-yl)glycine methyl esterHCID 13105389—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl esterHCID 20449787—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04465844
出典データセットuspto-grants-1984_08
ORD IDord-7f80ed19ce8148eea873befe7a1827be
出典メモuspto-grants-1984_08