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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702722Generated: October 31, 2026

Acetic Acid → HCID 70507526, compound

https://huagongshe.com/reaction/1702722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 131712816HCID 131712816—
CatalystZincHCID 23994—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70507526HCID 70507526—

Reaction Conditions

Temperature0 °C

Reaction Steps

The freshly prepared pivaloyloxymethyl 6-methoxy-2-methyl-1-oxo-6-(2-phenoxyacetamido)carbapen-2-em-3-carboxylate of Method B, Example 25, was dissolved in the minimum necessary tetrahydrofuran and added to a slurry of specially activated zinc powder (Example 2; 500 mg.) in a mixture of 1 ml. acetic acid and 0.5 ml. of tetrahydrofuran maintained at 0° C. After stirring for 1 hour at 0° C., the reaction mixture was diluted with toluene, evaporated to dryness in vacuo and chased several times with toluene. The residue was redissolved in methylene chloride, zinc removed by filtration, and the filtrate reconcentrated to dryness in vacuo. The residue was taken up in ether, insoluble impurities removed by filtration and the filtrate again evaporated to dryness in vacuo to yield pivaloyloxymethyl 6-methoxy-2-methyl-1-oxo-6-(2-phenoxyacetamido)carbapenam-3-carboxylate [20 mg.; Rf 0.70 (4:1 chloroform:ethyl acetate)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348264
Source datasetuspto-grants-1982_09
ORD IDord-4cf780d198f54a1eb7d777159b295061
Source noteuspto-grants-1982_09