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HRID 616157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/616157

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 acetatewater. 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US04072674
出典データセットuspto-grants-1978_02
ORD IDord-d504fd3780a844abb0c2b5ea5e1cea0d
出典メモuspto-grants-1978_02