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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163738Generated: November 1, 2026

1-Hexene → 5-Ethyl-2-Norbornene 1-Hexene

https://huagongshe.com/reaction/2163738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HexeneHCID 11597—
ReactantBicyclo(2.2.1)hept-2-ene, 5-ethyl-HCID 85837—
ReactantAlEt2IHCID 16686130—
SolventTolueneHCID 1140—
Product5-Ethyl-2-Norbornene 1-HexeneHCID 86736258—

Reaction Steps

50 ml dry toluene cosolvent, 7 ml 5-ethyl-2-norbornene, 0.8 ml 1-hexene solution, and 0.6 ml diethylaluminum iodide solution were charged to a dry, nitrogen-purged 7 oz. bottle. 0.75 ml of the MoCl5 solution was charged last, and the bottle was shaken. After 1 hour the reaction was shortstopped using a mixture of 0.8 ml ethanolamine, 3 ml Solution A and 25 ml toluene. 2 ml of an antioxidant solution was added (0.1 g/ml of 2,2'-methylenebis[4-methyl-6-t-butylphenol] in toluene). The polymer cement was coagulated using excess Solution A in a Waring blender. A solid weighing 5.9 grams was recovered after being filtered and vacuum dried at 60° C. It was found to be a ring-opened 5-ethyl-2-norbornene/1-hexene copolymer with a DSV of about 1.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04136248
Source datasetuspto-grants-1979_01
ORD IDord-ef4e22ac525f45cebddab40b6d5fc24d
Source noteuspto-grants-1979_01