HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707493Generated: November 3, 2026
Aluminum(III) Chloride → HCID 178482024, compound
https://huagongshe.com/reaction/1707493
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 141566131 | HCID 141566131 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 178482024 | HCID 178482024 | 70.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05352792 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-d6e99803edd44cbe967e917ccba9f463 |
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| Source note | uspto-grants-1994_10 |
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