Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183087Generated: November 1, 2026

4-Nitrobenzaldehyde → HCID 131724906, compound

https://huagongshe.com/reaction/2183087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantSodium IodideHCID 5238—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131724899HCID 131724899—
ReactantHCID 131724904HCID 131724904—
ProductHCID 131724906HCID 13172490650%

Reaction Steps

7-[2-tert-butoxycarbonylmethoxyimino-2-(2-tritylaminothiazol-4-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylic acid benzhydryl ester (470 mg, 0.5 mmol), sodium iodide (75 mg, 0.5 mmol), triphenylphosphine (131 mg, 0.5 mmol), 4-nitrobenzaldehyde (302 mg, 2 mmol) and sodium hydrogen carbonate (126 mg, 1.5 mmol) were used to conduct the procedure similar to that shown in (1) of Example 1 to obtain 260 mg (yield: 50%) of 7-[2-carboxymethoxyimino-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-171e8d87ca81409d90f342a41a1db9a5
Source noteuspto-grants-2005_05