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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195464Generated: October 30, 2026

Pyrophosphoric acid → HCID 178519397, compound

https://huagongshe.com/reaction/1195464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrophosphoric acidHCID 1023—
Reactant4-Chlorobenzoic AcidHCID 6318—
ReactantDichloromethaneHCID 6344—
ReactantBis(eta-cyclopentadienyl) ironHCID 7611—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 178519397HCID 17851939761%

Reaction Steps

5.30 of p-chlorobenzoic acid, 1.0 ml of triethylamine, and 2 ml of phosphorus oxychloride were added and stirred at 0° C. for 30 minutes with 40 ml of methylene chloride, and 60 ml of pyrophosphoric acid and 6.0 g of ferrocene were added. The resulting mixture was heat-refluxed, then poured into water, and made to be basic with sodium hydroxide, subjected to extraction with methylene chloride, and dried. Subsequently, the unreacted ferrocene was removed with column chromatography, to obtain 6.16 g of p-chlorophenylferrocenyl ketone represented by the formula (E), in a yield of 61.0%. The proton nuclear magnetic resonance (1H--NMR) spectrum of the product is shown in FIG. 5. The result showed that the resulting product was the desired compound (p-chlorophenylferrocenyl ketone). ##STR12##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110964
Source datasetuspto-grants-1992_05
ORD IDord-976b4655ebe048f498607ff4b39a97f3
Source noteuspto-grants-1992_05