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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707474Generated: October 30, 2026

Aluminum(III) Chloride → HCID 178508516, compound

https://huagongshe.com/reaction/1707474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 178452987HCID 178452987—
SolventNitromethaneHCID 6375—
SolventAnisoleHCID 7519—
ProductHCID 178508516HCID 17850851693.4%

Reaction Steps

To a suspension of 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2-trityloxyiminoacetamido]-3-(1,2,3-triazol-4-yl) thiomethylthio-3-cephem-4-carboxylic acid diphenylmethyl ester (9.2 g: 9 mMol.) in a mixture of anisole (18 ml) and nitromethane (72 ml) is added dropwise a solution of aluminum chloride (9.6 g: 72 mMol.) in anisole (31 ml) at -30° C. After stirring for 1 hour at the same temperature, the reaction mixture is quenched with ethanol (25 ml), stirred for several minutes, diluted with 1N-hydrochloric acid (75 ml) and water (500 ml), and washed with ethyl acetate. The aqueous layer was separated, concentrated to remove the organic solvents, and passed through a column of styrene-divinylbenzene copolymer adsorbent. The product is eluted with a mixture of methanol and water (4:1) to give 7β-[(Z)-2-(2-aminothiazol-4-yl)-2-hydroxyiminoacetamido]-3-(1,2,3-triazol-4-yl)thiomethylthio-3-cephem-4-carboxylic acid as pale yellow powder (4.19 g). Yield: 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352792
Source datasetuspto-grants-1994_10
ORD IDord-e6bed7ea83814f6899f3677782e7ee1f
Source noteuspto-grants-1994_10