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HRID 1903603作成日:2026年10月25日

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

https://huagongshe.com/reaction/1903603

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl esterHCID 20449787—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物2-[1-(2,4-Dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl]glycine methyl esterHCID 13105391—

反応手順

In a mixture of 50 ml of methanol and 5 ml of acetic acid was dissolved 3 g of benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl]glycine methyl ester and after addition of 500 mg of palladium black, the mixture was stirred in a stream of hydrogen at room temperature for 2.5 hours. The catalyst was filtered off and the filtrate was concentrated to dryness under reduced pressure. The concentrate was chromatographed on a silica gel column and eluted with toluene-acetone (4:1). The eluate was concentrated under reduced pressure and to the residue was added 100 ml of ethyl ether-petroleum ether (1:5). The mixture was allowed to stand in a refrigerator overnight and the resulting precipitate was collected by filtration and dried. Yield 1.4 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04436918
出典データセットuspto-grants-1984_03
ORD IDord-c166a984cb7443648e1b34c104485db9
出典メモuspto-grants-1984_03