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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885423Generated: November 2, 2026

Cyclopentadiene → HCID 53436388, compound

https://huagongshe.com/reaction/1885423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentadieneHCID 7612—
Reactantt-Butyl bromideHCID 10485—
ReactantPotassium HydroxideHCID 14797—
SolventPentaneHCID 8003—
ProductHCID 53436388HCID 53436388—

Reaction Steps

In this example, freshly distilled cyclopentadiene, a 50 wt % aqueous solution of potassium hydroxide, and tertiary-butyl bromide in the molar ratio of 1:40:5 were stirred together in a reactor. The quaternary ammonium halide, Adogen® 464 is added in the amount of one gram per mole of the potassium hydroxide. These reactants were stirred together and heated to 60° for 75 minutes and then at 100° for an additional 45 minutes. During the reaction foaming may occur which should be controlled. The reaction mixture is then cooled, diluted with pentane, washed with water and dried over magnesium sulfate. The pentane is then removed by vacuum. The crude residue contains the product and the Adogen® 464. Chromatography of the crude material over silica gel yielded di(tert-butyl)-cyclopentadiene. The overall calculated yield is 90 wt % based on the starting cyclopentadiene material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05144095
Source datasetuspto-grants-1992_09
ORD IDord-001f250499cf4fc9854864a62cc56371
Source noteuspto-grants-1992_09