Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707452Generated: October 31, 2026

Ethyl Acetate → HCID 70580077, compound

https://huagongshe.com/reaction/1707452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPhosphorus trichlorideHCID 24387—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178477301HCID 178477301—
SolventDimethylformamideHCID 6228—
ProductHCID 70580077HCID 70580077267.7%

Reaction Steps

To a solution of 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-trityloxyiminoacetylamino]-3-(1-methyl-1,2,4-triazol-3-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester 1-oxide (1.78 g: 1.69 mMol.) in dimethylformamide (15 ml) at -20° C. is added phosphorus trichloride (0.42 ml: 4.18 mMol.), and the mixture is stirred at the same temperature for 20 minutes. The reaction mixture is poured into two layers of cold aqueous sodium hydrogen carbonate and ethyl acetate. The organic layer is taken, washed with water and brine, dried over sodium sulfate, and concentrated. The residue is purified by silica gel chromatography (toluene: ethyl acetate=2:1) to give 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-trityloxyiminoacetamido]-3-(]-methyl-1,2,4-triazol-3-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester (1.59 g) as brown foam. Yield: 91%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352792
Source datasetuspto-grants-1994_10
ORD IDord-e5e50ecd2b1544f080deda22818f8228
Source noteuspto-grants-1994_10