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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596832Generated: October 30, 2026

Acetone → Benzhydryl 7-(2-thienylacetamido)-3-acetyl-2-cephem-4-carboxylate

https://huagongshe.com/reaction/596832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantChromic AcidHCID 24425—
ReactantHCID 70617653HCID 70617653—
SolventIsopropanolHCID 3776—
ProductBenzhydryl 7-(2-thienylacetamido)-3-acetyl-2-cephem-4-carboxylateHCID 7063600171.2%

Reaction Steps

To a stirred solution of 2.98 g. of benzhydryl 7-(2-thienylacetamido)-3-(1-hydroxyethyl)-2-cephem-4-carboxylate in 200 ml. of acetone was added dropwise 2.83 ml. of a 2.26 molar chromic acid solution. The reaction mixture was allowed to stir at room temperature for ten minutes, after which time approximately 10 ml. of isopropanol was added. The reaction mixture was stirred for 5 minutes and then evaporated in vacuo to dryness. The residue was taken up in a mixture of ethyl acetate and water and transferred to a separatory funnel with the aid of ethyl acetate. The organic layer was separated and washed successively with brine (4X), sodium bicarbonate solution, water, 1N.HCl, and brine (2X) and then dried over anhydrous sodium sulfate. The residue obtained upon evaporation in vacuo of the solution thereby obtained was chromatographed on a silica gel column using a toluene-ethyl acetate gradient to provide 2.11 g. (71.2 percent) of the title product:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012380
Source datasetuspto-grants-1977_03
ORD IDord-3e4771adabd64312a2f2d02b5ec512f8
Source noteuspto-grants-1977_03