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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707493Generated: November 3, 2026

Aluminum(III) Chloride → HCID 178482024, compound

https://huagongshe.com/reaction/1707493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 141566131HCID 141566131—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventNitromethaneHCID 6375—
SolventAnisoleHCID 7519—
ProductHCID 178482024HCID 17848202470.2%

Reaction Steps

To a solution of 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-trityloxyiminoacetyl]amino-3-(1-methyl-5-tetrazolyl)thiomethylthio-3-cephem-4-carboxylic acid diphenylmethyl ester (576 mg: 0.555 mMol.) in a mixture of anisole (2 ml) and nitromethane (8 ml) cooling at -30° to -40° C. is added a solution of aluminum chloride (591 mg: 4.44 mMol.) in anisole (2 ml), and the mixture is stirred at -30° to -40° C. for 1 hour. The reaction mixture is diluted with 1N-hydrochloric acid (5 ml) and water and washed with ethyl acetate. The aqueous layer is concentrated under reduced pressure to remove the organic solvents, and purified by styrene-divinylbenzene copolymer chromatography (methanol: water=4:1). The resulting powder is washed with ethyl acetate to give 7β-[(Z)-2-(2-aminothiazol-4-yl)-2-hydroxyiminoacetyl]amino-3-(1-methyl-5-tetrazolyl)thiomethylthio-3-cephem-4-carboxylic acid as yellow powder (200 mg). Yield: 68%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352792
Source datasetuspto-grants-1994_10
ORD IDord-d6e99803edd44cbe967e917ccba9f463
Source noteuspto-grants-1994_10