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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413813Generated: October 29, 2026

Carbon tetrabromide → Benzhydryl 7-phenylacetamido-3-(2,2-dibromovinyl)-2-cephem-4-carboxylate

https://huagongshe.com/reaction/2413813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantHCID 88626080HCID 88626080—
CatalystZincHCID 23994—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBenzhydryl 7-phenylacetamido-3-(2,2-dibromovinyl)-2-cephem-4-carboxylateHCID 8860099333.7%

Reaction Steps

To a stirred mixture of triphenylphosphine (40.7 g) and zinc powder (18.5 g) in methylene chloride (250 ml) was added carbontetrabromide (45 g) at 20°-30° C. Benzhydryl 7-phenylacetamido-3-formyl-2-cephem-4-carboxylate (10 g) was added portionwise to the above reaction mixture, and the mixture was stirred for 30 minutes at room temperature. Triphenylphosphine oxide was solidified by addition of ethyl acetate to the reaction mixture and removed by filtration. The residue left by removal of the solvents was chromatographed on silica gel. The elution with chloroform containing ethyl acetate (10%) gave benzhydryl 7-phenylacetamido-3-(2,2-dibromovinyl)-2-cephem-4-carboxylate (4.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719206
Source datasetuspto-grants-1988_01
ORD IDord-b0040f1cab25468493caf6878cc7dd83
Source noteuspto-grants-1988_01