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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195463Generated: October 31, 2026

Pyrophosphoric acid → HCID 178520530, compound

https://huagongshe.com/reaction/1195463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrophosphoric acidHCID 1023—
ReactantBis(eta-cyclopentadienyl) ironHCID 7611—
ReactantButyl etherHCID 8909—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromobutyric acidHCID 75809—
SolventWaterHCID 962—
ProductHCID 178520530HCID 17852053082.1%

Reaction Steps

6.68 g of 4-bromobutyric acid, 1.86 g of ferrocene, 20 g of pyrophosphoric acid, 20 g of polyphosphoric acid, and 20 ml of di n-butylether were added and stirred while heating at 50° to 60° C. for 3 hours, then poured into water, made to be basic with sodium hydroxide, extracted with methylene chloride, and dried. The unreacted-ferrocene was removed with column chromatography, to obtain 2.75 g of 3-bromopropylferrocenyl ketone presented by the formula (D), in a yield of 82.0%. The proton nuclear magnetic resonance (1H--NMR) spectrum of the product is shown in FIG. 4. The result showed that the resulting product was the desired product (3-bromopropylferrocenyl ketone). ##STR11##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110964
Source datasetuspto-grants-1992_05
ORD IDord-8c690e8881d14c39aeb12f0f8e770b4a
Source noteuspto-grants-1992_05