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HRID 258009作成日:2026年10月27日

Hydrogen Peroxide → p-Methoxybenzyl 7beta-amino-3-azidomethyl-3-cephem-4-carboxylate-1,1-dioxide

https://huagongshe.com/reaction/258009

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Sodium SulfiteHCID 24437—
反応物p-Methoxybenzyl 7beta-amino-3-azidomethyl-3-cephem-4-carboxylateHCID 131718254—
触媒Sodium Tungstate DihydrateHCID 150191—
溶媒Ethyl AcetateHCID 8857—
生成物p-Methoxybenzyl 7beta-amino-3-azidomethyl-3-cephem-4-carboxylate-1,1-dioxideHCID 131718253—

反応手順

p-Methoxybenzyl 7β-amino-3-azidomethyl-3-cephem-4-carboxylate (17.15 g, 0.046 mol) in ethyl acetate was cooled to 15° C., sodium tungstate dihydrate (1.52 g, 0.0046 mol) was added followed by hydrogen peroxide (30%, 20.73 ml) in one portion and the stirring was continued at room temperature. After two hours an additional portion of hydrogen peroxide (5.18 ml) was added and the reaction mixture was stirred at room temperature for a total period of 18 h; the mixture was cooled to 10° C. and a solution of sodium sulphite (10%, 600 ml) was added while stirring. Organic layer was separated out, washed with aq. sodium bicarbonate solution, brine and dried (Na2SO4). Evaporation of the solvent in vacuo gave a foam (12 g) which was purified over a silica column using hexane-ethyl acetate (1:3) as eluant to give the pure product as a white foam (6.8 g, 36.5%). IR (Nujol) ν max 2083 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05264429
出典データセットuspto-grants-1993_11
ORD IDord-4181c31959a440168d9c37b195912fba
出典メモuspto-grants-1993_11