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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654632Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 178494566, compound

https://huagongshe.com/reaction/1654632

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 14459633HCID 14459633—
SolventEthanolHCID 702—
ProductHCID 178494566HCID 178494566—

Reaction Steps

A solution of 2.1 g (11 mmol ) of p-toluenesulfonic acid in 5 ml of ethanol was added dropwise to a solution of 5 g (9.3 mmol) of α-(2,2-dimethylpropanoyloxy)ethyl 7-[2-(2-aminothiazol-4-yl)-2-(Z)-hydroxyimino-acetamido]-3-methoxymethyl-3-cephem-4-carboxylate in 32 ml of ethanol. After stirring at room temperature for 30 minutes, a total of 280 ml of diisopropyl ether were added to the crystal magma formed and the mixture was briefly stirred. The precipitate formed was then filtered off with suction and washed with a little diisopropyl ether, and the residue was dried in vacuo over calcium chloride/paraffin. 5.4 g of the desired crystalline title compound were obtained, which consisted of an approximately 1:1 mixture of the two diastereomers according to HPLC and was identical in its physical and chemical properties with the product from working example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409918
Source datasetuspto-grants-1995_04
ORD IDord-18c7b84009e74d12989c1e6d1c325065
Source noteuspto-grants-1995_04