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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616157Generated: October 26, 2026

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

https://huagongshe.com/reaction/616157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium Phosphate, DibasicHCID 24203—
ReactantPotassium PersulfateHCID 24412—
ReactantMethyl 3-t-butoxycarbonylamino-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylateHCID 23470103—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductMethyl cis-3-t-butoxycarbonylamino-4-oxoazetidine-2-carboxylateHCID 7042837231%

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072674
Source datasetuspto-grants-1978_02
ORD IDord-d504fd3780a844abb0c2b5ea5e1cea0d
Source noteuspto-grants-1978_02