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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955394Generated: October 31, 2026

Cyclopentadiene → HCID 53851949, compound

https://huagongshe.com/reaction/1955394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentadieneHCID 7612—
Reactant2-BromopentaneHCID 7890—
ReactantSodium HydroxideHCID 14798—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
ProductHCID 53851949HCID 53851949—

Reaction Conditions

Temperature70 °C

Reaction Steps

A double-walled reactor having a volume of 1 L, provided with baffles, condenser, top stirrer, thermometer and dropping funnel was charged with 900 g (11.25 mol) of clear 50% strength NaOH. Then 31 g of Aliquat 336 (77 mmol) and 26.8 g (0.41 mol) of freshly cracked cyclopentadiene were added. The reaction mixture was stirred turbulently for a few minutes. Then 155 g of 2-pentyl bromide (1.03 mol) were added over a period of 1 hour, cooling with water taking place at the same time. After 3 hours' stirring at room temperature the reaction mixture was warmed to 70° C., followed by a further 2 hours' stirring. Stirring was stopped and phase separation was awaited. The water layer was drawn off and 900 g (11.25 mol) of fresh 50% strength NaOH were added, followed by a further two hours' stirring at 70° C. GC was used to show that at that instant the mixture consisted of di- and tri(2-pentyl)cyclopentadiene (approximately 1:1). The products were distilled at 2 mbar, 79-81° C. and 0.5 mbar, 102° C., respectively. After distillation, 28 g of di- and 40 g of tri(2-pentyl)cyclopentadiene were obtained. Characterization took place with the aid of GC, GC-MS, 13C- and 1H-NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124488
Source datasetuspto-grants-2000_09
ORD IDord-e56513df928a4189bc143b45667eb663
Source noteuspto-grants-2000_09