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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978907Generated: October 30, 2026

Isopropanol → HCID 86740487, compound

https://huagongshe.com/reaction/978907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant(6R,7S)-7-Azido-2,2-dimethyl-3-oxa-1-azabicyclo[4.2.0]octan-8-oneHCID 71403629—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
ProductHCID 86740487HCID 86740487—

Reaction Steps

In 30 ml of acetone is dissolved 330 mg of trans-2,2-dimethyl-7-azido-1-aza-3-oxabicyclo[4.2.0]octan -8-one and under ice-cooling and stirring, 3.3 ml (8N solution) of Jones reagent is added. The mixture is stirred for 2.5 hours, after which 5 ml of isopropyl alcohol is added and the mixture is further stirred for 10 minutes. The insolubles are filtered off with the aid of Celite and the filtrate is concentrated under reduced pressure. The residue is shaken with tetrahydrofuran and a small amount of saturated aqueous sodium chloride. The tetrahydrofuran layer is taken and extracted three times with tetrahydrofuran. The tetrahydrofuran layers are combined, dried over anhydrous sodium sulfate and, after addition of a solution of diazomethane in ether, the mixture is allowed to stand. The solvent is then distilled off and the residue is shaken with water and ethyl acetate. The ethyl acetate layer is taken, washed with aqueous sodium hydrogen carbonate and water in this order and dried over anhydrous sodium sulfate. It is concentrated under reduced pressure and the residue is purified by silica gel column chromatography to give trans-3-azido-4-methoxycarbonylmethyl-2-oxoazetidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665067
Source datasetuspto-grants-1987_05
ORD IDord-d50d740d22504456975c4f9c501cece1
Source noteuspto-grants-1987_05