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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127645Generated: October 30, 2026

Toluene → HCID 178520257, compound

https://huagongshe.com/reaction/127645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 131712126HCID 131712126—
SolventDichloromethaneHCID 6344—
ProductHCID 178520257HCID 178520257—

Reaction Steps

A solution of 0.96 g (1.62 mmols) of 7β-phenylacetylamino-3-phenylthio-3-cephem-4-carboxylic acid diphenylmethyl ester and 0.26 ml (2.43 mmols) of anisole in 9.6 ml of methylene chloride is stirred with 1.24 ml (16.2 mmols) of trifluoroacetic acid for 30 minutes at 0° C. and the mixture is treated with 50 ml of cold toluene and evaporated in vacuo and the residue is dried in a high vacuum. The residue is digested with diethyl ether, filtered off, rinsed with the same solvent and dried in vacuo. 7β-Phenylacetylamino-3-phenylthio-3-cephem-4-carboxylic acid is obtained as a microcrystalline, colourless powder which can be recrystallised from acetone/methylene chloride/diethyl ether. Melting point 190° C. (decomposition). Thin layer chromatogram (silica gel): Rf ~0.60 (n-butanol/pyridine/acetic acid/H2O, 40:24:6:30); UV spectrum (ethanol): λmax =263 nm (ε=7000); 305 nm (ε=9000); IR spectrum (nujol): characteristic bands at 3.02; 5.59; 5.81; 6.01; 6.22 and 6.48μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256739
Source datasetuspto-grants-1981_03
ORD IDord-d0e9536f40364e58b669912f70b6e954
Source noteuspto-grants-1981_03