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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296548Generated: October 31, 2026

Acetic Acid → HCID 13065657, compound

https://huagongshe.com/reaction/2296548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 13065655HCID 13065655—
CatalystNickelHCID 935—
CatalystZincHCID 23994—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 13065657HCID 13065657—

Reaction Steps

Pivaloyloxymethyl 2-methyl-1-oxocarbapen-2-em-3-carboxylate, freshly prepared from 50 mg. of pivaloyloxymethyl 1-beta-oxo-2-diazo-3-methylceph-3-em-4-carboxylate by the method of Example 1 (employing the alternative Raney nickel step), was taken up in approximately 0.25 ml. of tetrahydrofuran and added to a slurry of 500 mg. of zinc powder, specially activated by the method of Rieke and Uhm [Synthesis, 452 (1975)], in 15 ml. of acetic acid-30% tetrahydrofuran at 0° C. After stirring for 1 hour at this temperature, the reaction mixture was diluted with toluene, stripped in vacuo and the residue chased several times with toluene. The vacuum pumped residue was taken up in excess methylene chloride, the zinc removed by filtration, and the filtrate reevaporated in vacuo to yield essentially homogeneous pivaloyloxymethyl 2-methyl-1-oxocarbapenam-3-carboxylate (tlc: Rf 0.45 with 18:1 chloroform:ethyl acetate as eluant; ir 1780, 1760 cm-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429128
Source datasetuspto-grants-1984_01
ORD IDord-9ac472b75bf0406e999fc2930446d501
Source noteuspto-grants-1984_01