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HRID 1862876作成日:2026年10月26日

Sodium Phosphate, Dibasic → Methyl cis-3-t-butoxycarbonylamino-4-oxoazetidine-2-carboxylate

https://huagongshe.com/reaction/1862876

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium Phosphate, DibasicHCID 24203—
反応物Potassium PersulfateHCID 24412—
反応物Methyl 3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylateHCID 23470103—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物Methyl cis-3-t-butoxycarbonylamino-4-oxoazetidine-2-carboxylateHCID 7042837231%

反応手順

A solution of 10.5 g (26.7 mmole) of methyl 3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate in 500 ml of acetonitrile is degassed with argon and warmed to 80°. A degassed solution of 15 g (55.5 mmole) of potassium persulfate and 7.5 g (28 mmole) of sodium monohydrogen phosphate in 150 ml of water is added in five portions over 1 hr. The reaction is stirred at 80°-85° under argon for 2-3 hrs until all starting material is consumed (tlc). The reaction mixture is cooled, concentrated in vacuum, shaken with ethyl acetate-water. The organic phase is washed with dilute HCl, NaHCO3 solution and brine; dried over magnesium sulfate and evaporated to dryness. The residue is chromatographed over silica gel with 1:1 benzene-ethyl acetate to afford pure product which crystallized from ethyl acetate-hexane to yield 2.0 g (31%) of the title compound. A less pure fraction from the column, is crystallized from ethyl acetate-hexane to give an additional 0.5 g of product, overall yield, 38%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04166816
出典データセットuspto-grants-1979_09
ORD IDord-de6200806e6042ff9296c69c5dd354c7
出典メモuspto-grants-1979_09