Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702721Generated: October 29, 2026

Chloroform → HCID 70507140, compound

https://huagongshe.com/reaction/1702721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantHCID 70507631HCID 70507631—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 70507140HCID 70507140—

Reaction Steps

Benzhydryl 1-acetoxy-2-methyl-6-(2-phenoxyacetamido)carbapenam-3-carboxylate (18 mg.) was dissolved in 3 ml. of ethyl acetate. Hydrogenation catalyst (18 mg. of 10% palladium on carbon) was added and the mixture hydrogenated at atmospheric pressure and room temperature for 1 hour. When tlc (4:1 chloroform:ethyl acetate) indicated no change, a second aliquot of catalyst (18 mg.) was added. According to tlc assay, some conversion occurred during the next hour, at which time a third aliquot of catalyst (18 mg.) was added. At the end of another hour of hydrogenation, tlc assay indicated reduction to be complete. Catalyst was recovered by filtration with ethyl acetate wash. The combined filtrate and washes were evaporated to dryness in vacuo to yield 1-acetoxy-2-methyl-6-(2-phenoxyacetamido)carbapenam-3-carboxylic acid [Rf 0.77 (18:1 acetone:water); ir (CH2Cl2) 1775, 1725, 1675 cm-1 ].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348264
Source datasetuspto-grants-1982_09
ORD IDord-1eaf64d6c8b74518acb20f3f55e49b2f
Source noteuspto-grants-1982_09