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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461945Generated: October 27, 2026

p-Toluenesulfonic acid → p-Nitrobenzyl 7-amino-3-methylenecepham-4-carboxylate p-toluenesulfonate

https://huagongshe.com/reaction/461945

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantDichloromethaneHCID 6344—
ReactantPhosphorus pentachlorideHCID 24819—
Reactantp-Nitrobenzyl 7-Penoxyacetamido-3-methylenecepham-4-carboxylateHCID 20837924—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
Productp-Nitrobenzyl 7-amino-3-methylenecepham-4-carboxylate p-toluenesulfonateHCID 131710312—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 965 mg. of p-nitrobenzyl 7-phenoxyacetamido-3-methylenecepham-4-carboxylate in 10 ml. of methylene chloride were added 175 mg. of dry pyridine and 460 mg. of phosphorus pentachloride and the mixture was stirred for five hours at room temperature. Thereafter the reaction mixture was cooled to 0° C. and 50 ml. of cold methanol were added. Following a stirring period of one-hour at room temperature the reaction mxture was evaporated in vacuo to remove the solvents and the residual reaction product mixture was dissolved in a mixture of ethyl acetate and water. The pH was adjusted to pH 7 and the ethyl acetate layer was separated and was washed with water and dried. One equivalent of p-toluene sulfonic acid was added to the dried solution and on cooling 600 mg. of p-nitrobenzyl 7-amino-3-methylenecepham-4-carboxylate p-toluenesulfonate formed as a crystalline precipitate. The product was purified by recrystallization from a mixture of 12 ml. of methanol 24 ml. of ether and 15 ml. of petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064343
Source datasetuspto-grants-1977_12
ORD IDord-2dff9e7f54084207adcc489bae9a3f10
Source noteuspto-grants-1977_12