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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735297Generated: November 1, 2026

1,3-Cyclopentadiene, 1-propyl → HCID 178440519, compound

https://huagongshe.com/reaction/735297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Cyclopentadiene, 1-propylHCID 528171—
ReactantEinecs 254-460-4HCID 10269745—
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418365HCID 178418365—
ReactantHCID 178440518HCID 178440518—
ReactantHCID 178506698HCID 178506698—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178440519HCID 17844051912.8%

Reaction Conditions

Temperature-70 °C

Reaction Steps

80.0 g (223 mmol) of tantalum pentachloride was suspended in 1,340 ml of ether, and 324 ml (220 mmol) of isopropyl magnesium bromide (0.68M THF solution) was added thereto. A solution of 50.2 g (440 mmol) of propylcyclopentadienyl lithium prepared from propylcylopentadiene and butyl lithium in THF (380 ml) was added, followed by refluxing for 1 hour. The solvent was distilled away, and the residue was dried at 80° C. in vacuo for 8 hours to obtain a brownish-red solid containing dichlorobis(propylcyclopentadienyl)tantalum (Ta (PrCp)2Cl2). 2,100 ml of toluene was added to this brownish-red solid, and the resulting mixture was ice-cooled. 198 ml (660 mmol) of a toluene solution (65 wt %) of sodium bis(2-methoxyethoxy)aluminum hydride was added dropwise to the mixture, and temperature was returned to room temperature, followed by stirring for 19.5 hours. 106 ml of water was added to the mixture, followed by stirring until foaming does not occur. Insoluble contents were filtered out, and the solvent was distilled away from the filtrate. 2,000 ml of hexane was added to the residue, the insoluble contents were filtered out, and the filtrate was concentrated to about 800 ml. When the concentrated liquid was cooled to −70° C., a white solid was formed. A supernatant was removed, and the solid was washed with 40 ml of cold pentane two times to obtain 11.2 g (yield: 12.8%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592471B2
Source datasetuspto-grants-2009_09
ORD IDord-2f8e4317321b4a978412bc900f9ff358
Source noteuspto-grants-2009_09