Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414681Generated: November 3, 2026

Trifluoroacetic acid → HCID 88819429, compound

https://huagongshe.com/reaction/1414681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHeptaneHCID 8900—
ReactantHCID 88819802HCID 88819802—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductHCID 88819429HCID 88819429—

Reaction Steps

To a cooled (5°) stirred solution of 68 mg. of benzhydryl 7-(2-thienylacetamido)-3-(phenylthio)carbonylamino-3-cephem-4-carboxylate in 1 ml. of anisole was added 1 ml. of cold trifluoroacetic acid. The reaction mixture was allowed to stir with cooling for 20 minutes after which time was added approximately 30 ml. of n-heptane. The resulting solution was evaporated in vacuo to a low volume. An additional 5 ml. of n-heptane was added, and the resulting solution was stirred in an ice bath for 5 minutes. The solution was filtered, and the precipitate thereby obtained was dissolved in acetone. The acetone solution was then filtered, and the filtrate evaporated in vacuo to dryness. The solution obtained by dissolving the residue in ethyl acetate was extracted twice with aqueous sodium bicarbonate solution. The aqueous extracts were combined, layered with cold ethyl acetate and acidified with cold 1N.HCl. The ethyl acetate layer was separated, washed with brine, dried over anhydrous sodium sulfate, and evaporated in vacuo to dryness to provide 33 mg. of the title product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001226
Source datasetuspto-grants-1977_01
ORD IDord-50d94f3fab5348f09efc6a471772652d
Source noteuspto-grants-1977_01