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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953374Generated: November 1, 2026

Cyclopentadiene → HCID 14094221, compound

https://huagongshe.com/reaction/1953374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentadieneHCID 7612—
Reactant1-BromooctaneHCID 8140—
ReactantSodium HydroxideHCID 14798—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
ProductHCID 14094221HCID 14094221—

Reaction Conditions

Temperature10 °C

Reaction Steps

A double-walled reactor having a volume of 1.5 L, provided with baffles, condenser, top stirrer, thermometer and dropping funnel was charged with 900 g of clear 50% strength NaOH (11.3 mol), followed by cooling to 10° C. Then 30 g of Aliquat 336 (74 mmol) and 48 g (0.72 mol) of freshly cracked cyclopentadiene were added. The reaction mixture was stirred turbulently for a few minutes. Then 577 g of octyl bromide (2.99 mol) were added in one hour's time, cooling with water taking place at the same time. After 1 hour's stirring at room temperature the reaction mixture was heated to 35° C., followed by a further 6 hours' stirring. Stirring was stopped and phase separation was awaited. The water layer was drawn off and 920 g (11.5 mol) of fresh 50% strength NaOH were added, followed by a further 5 hours' stirring at room temperature. GC was used to show that at that instant 10% of tri-, 83% of tetra- and 7% of penta(octyl)cyclopentadiene were present in the mixture. The product was distilled at reduced pressure. After vacuum distillation, 226.6 g of tetra(octyl)cyclopentadiene were obtained. Characterization of the product took place with the aid of GC, GC-MS, 13C- and 1H-NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117811
Source datasetuspto-grants-2000_09
ORD IDord-7d212898f1fd439082bb3cb461a580ce
Source noteuspto-grants-2000_09