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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448404Generated: October 30, 2026

Methanol → HCID 178431946, compound

https://huagongshe.com/reaction/1448404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 70604893HCID 70604893—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178431946HCID 17843194651%

Reaction Steps

A mixture of 100 mg. (1 mmole) of potassium bicarbonate and 2.3 g. of 10% palladium-on-carbon, in a mixture of 12 ml. of methanol and 3 ml. of water, is stirred under an atmosphere of hydrogen until hydrogen uptake ceases. A solution of 464 mg. of 6-(2-phenoxyacetamido)-2,2-dimethyl-3-(1-benzyltetrazol-5-yl)penam in 10 ml. of ethyl acetate is then added, and stirring under an atmosphere of hydrogen is continued for an additional 5 hours. At this point the reaction mixture is filtered, and the residue is washed with aqueous methanol. The washings and the filtrate are combined and evaporated in vacuo. To this latter residue is added chloroform and water and the pH is adjusted to 8.0. The chloroform is removed and discarded, and fresh chloroform is added to the aqueous phase. The pH is lowered to 2.5 and the chloroform layer is separated. The dried chloroform is evaporated in vacuo, leaving 190 mg. (51% yield) of 6-(2-phenoxyacetamido)-2,2-dimethyl-3 -(5-tetrazolyl)penam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179511
Source datasetuspto-grants-1979_12
ORD IDord-c2d379f9e3284cbfb52eee38ecf0a450
Source noteuspto-grants-1979_12