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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050382Generated: November 1, 2026

Sodium Chloride → HCID 70579374, compound

https://huagongshe.com/reaction/2050382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl cis-3-phenoxyacetamido-4-oxoazetidine-2-carboxylateHCID 53649703—
ReactantHCID 178418361HCID 178418361—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70579374HCID 70579374—

Reaction Steps

To a solution of 13.5 g (0.049 mole) of methyl cis-4-oxo-3-phenoxyacetylaminoazetidine-2-carboxylate in 975 ml of tetrahydrofuran and 100 ml of water at 0° (ice bath) was added a cold solution of 3.75 g (0.099 mole) of sodium borohydride in 250 ml of water over a period of 10 min. The solution was stirred at 0° for 40 min and then glacial acetic acid was added dropwise until hydrogen evolution ceased. Solid sodium bicarbonate and sodium chloride were added and this mixture was extracted five times with 250 ml portions of ethyl acetate. After drying the combined extracts (MgSO4), the solvent was removed in vacuo. The resulting residue was dissolved in ethyl acetate, clarified with Norite and allowed to crystallize to give the title compound; tlc: ethyl acetate, silica gel GF, Rf=0.10; mp 153°-154° (ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200572
Source datasetuspto-grants-1980_04
ORD IDord-2c25cef5009a4b1f9e422fbbc4effbca
Source noteuspto-grants-1980_04