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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183081Generated: November 3, 2026

4-Nitrobenzaldehyde → HCID 131724897, compound

https://huagongshe.com/reaction/2183081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantSodium IodideHCID 5238—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131724898HCID 131724898—
ReactantHCID 131724899HCID 131724899—
ProductHCID 131724897HCID 13172489766.5%

Reaction Steps

7-[2-(1-methyl-1-tert-butoxycarbonylethoxyimino)-2-(2-tritylaminothiazol-4-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylic acid benzhydryl ester (775 mg, 0.8 mmol), sodium iodide (120 mg, 0.8 mmol), triphenylphosphine (210 mg, 0.8 mmol), 4-nitrobenzaldehyde (483 mg, 3.2 mmol) and sodium hydrogen carbonate (200 mg, 2.4 mmol) were used to conduct the procedure similar to that shown in (1) of Example 1 to obtain 568 mg (yield: 66%) of 7-[2-(1-methyl-1-tert-butoxycarbonylethoxyimino)-2-(2-tritylaminothiazol-4-yl)acetamido]-3-(4-nitrostyryl)-3-cephem-4-carboxylic acid benzhydryl ester as yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897304B2
Source datasetuspto-grants-2005_05
ORD IDord-d646fec045754c5a84f3dee3aeb39eed
Source noteuspto-grants-2005_05