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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461600Generated: October 31, 2026

Water → HCID 67796345, compound

https://huagongshe.com/reaction/1461600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphoric AcidHCID 1004—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant(3S,4S)-4-(1-chloromethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinoneHCID 67796056—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 67796345HCID 67796345—

Reaction Steps

To a solution of (3S,4S)-4-(1-chloromethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone (20 g) in dimethylsulfoxide (160 ml) were successively added water (40 ml), cuprous oxide (6.76 g) and p-toluenesulfonic acid (7.6 g), and the resultant mixture was warmed to 50° to 55° C. and stirred for 2 hours at the same temperature. After cooling down to room temperature, 1% aqueous phosphoric acid (90 ml) and ethyl acetate (200 ml) were poured into the reaction mixture, followed by stirring for 0.5 hour. An insoluble material was removed by filtration over celite and washed 3 times with ethyl acetate (20 ml). The filtrate and the washings were combined together, and the aqueous layer was separated from the organic layer and the extract were combined together, washed with brine and dried over anhydrous sodium sulfate. After filtration and concentration of the filtrate in vacuo, the concentrate was crystallized from a mixture of toluene and n-hexane (1:1) to give crystals of (3S,4S)-4-(1-hydroxymethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)- 1-di(p-anisyl)methyl-2-azetidinone. m.p., 118°-120 ° C. ##STR31##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075435
Source datasetuspto-grants-1991_12
ORD IDord-7b3222765cfb4338ad0e394ebc7cd264
Source noteuspto-grants-1991_12