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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033457Generated: November 2, 2026

Hydrochloric Acid → HCID 15223720, compound

https://huagongshe.com/reaction/1033457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron trifluorideHCID 6356—
ReactantSodium BicarbonateHCID 516892—
Reactant(3S,4S)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4-[(1R)-1-p-methoxybenzyloxycarbonylethyl]-1-(p-nitrobenzyloxycarbonylmethyl)azetidin-2-oneHCID 15223718—
SolventDichloromethaneHCID 6344—
ProductHCID 15223720HCID 15223720—
ProductHCID 15223722HCID 15223722—

Reaction Steps

To a solution of (3S,4S)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4-[(1R)-1-p-methoxybenzyloxycarbonylethyl]-1-(p-nitrobenzyloxycarbonylmethyl)azetidin-2-one (142 mg) in dry methylene chloride, there was BF3 --Et2O complex (163 mg) under ice-cooling, followed by stirring at room temperature. The reaction mixture was poured into a cold aqueous sodium bicarbonate solution, acidified with dilute hydrochloric acid and extracted with ethyl acetate three times. The organic layer was washed successively with dilute hydrochloric acid and brine, dried over sodium sulfate and evaporated., The residue was purified by silica gel chromatography to give (3S,4S)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4-[(1R)-1-carboxyethyl]-1-(p-nitrobenzyloxycarbonylmethyl)azetidin-2-one (Compound A) and (3S,4S)-3-[(1R)-1-hydroxyethyl]-4-[(1R)-1-carboxyethyl]-1-(p-nitrobenzyloxycarbonylmethyl)azetidin-2-one (Compound B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310897
Source datasetuspto-grants-1994_05
ORD IDord-85af8eb9eedd4c59add77bfdd51651be
Source noteuspto-grants-1994_05