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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707449Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → HCID 178452986, compound

https://huagongshe.com/reaction/1707449

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 88448825HCID 88448825—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductHCID 178452986HCID 17845298631%

Reaction Steps

To a solution of 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-trityloxyiminoacetylamino]-3-(trityl-1,2,4-triazol-3-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester 1-oxide (11.3 g) in acetone (60 ml) under ice cooling is added toluene-p-sulfonic acid monohydrate (1.68 g: 8.83 mMol.), and the mixture is stirred at room temperature for 4 hours. The reaction mixture is diluted with ethyl acetate, washed with aqueous 5% sodium hydrogen carbonate and brine, dried over sodium sulfate, and concentrated. The residue is purified by silica gel chromatography (toluene: ethyl acetate=1:1-1:2) to give 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-trityloxyiminoacetylamino]-3-(1,2,4-triazol-3-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester 1-oxide (2.84 g) as brown foam. Yield: 31%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352792
Source datasetuspto-grants-1994_10
ORD IDord-e502540090b547ae8d42a1a214f43d9c
Source noteuspto-grants-1994_10