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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482846Generated: October 30, 2026

Hydrochloric Acid → HCID 20559124, compound

https://huagongshe.com/reaction/482846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20243661HCID 20243661—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 20559124HCID 2055912441%

Reaction Steps

A mixture of methyl 2-(3-azido-4-formyl-2-oxo-1-azetidinyl)-2-phenylacetate (2.30 g.), sodium borohydride (310 mg), ethanol (40 ml.) and water (5 ml.) was stirred at -10° to 0° C. for an hour. The reaction mixture was adjusted to pH 4 to 5 with 10% hydrochloric acid at the same temperature, whereafter the ethanol was removed by distillation from the solution to give an aqueous residue, to which sodium chloride was added. The resultant solution was extracted twice with chloroform and the extract was washed with an aqueous sodium chloride. After drying the solution over magnesium sulfate, the solution was evaporated to dryness under reduced pressure to give a residue(2.02 g.), which was subjected to column chromatography on alumina(20 g.). Elution was carried out with chloroform and the fractions containing a desired compound were collected. The solvent was removed by distillation under reduced pressure to give methyl 2-(3-azido-4-hydroxymethyl-2-oxo-1-azetidinyl)-2-phenylacetate(0.95 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576753
Source datasetuspto-grants-1986_03
ORD IDord-f7aa1facfd654a278fc05447ef67fc42
Source noteuspto-grants-1986_03