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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163740Generated: October 27, 2026

1-Butene → Norbornene 1-Butene

https://huagongshe.com/reaction/2163740

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButeneHCID 7844—
Reactant2-NorborneneHCID 10352—
ReactantAlEt2IHCID 16686130—
SolventBenzeneHCID 241—
ProductNorbornene 1-ButeneHCID 86736257—

Reaction Steps

500 ml dry benzene cosolvent, 77 ml 2-norbornene solution, 10 ml of the 1-butene solution, and 6 ml of the diethylaluminum iodide solution were charged to a dry, nitrogen-purged quart bottle. 7.5 ml of the MoCl5 solution was charged last, and the bottle was shaken. Polymerization occurred so rapidly that the reaction was terminated after 7-8 minutes using a mixture of 1.5 ml ethanolamine, 10 ml of an antioxidant solution (10 grams of 2,2',2"-tris[3(3,5-di-t-butyl-4-hydroxyphenyl) propionyloxy] ethyl isocyanurate in 100 ml benzene) and 1 ml ethanol. The polymer cement was allowed to stand for about 12 hours and coagulated using excess Solution A in a Waring blender. A slightly yellow solid formed and was filtered and vacuum dried at 60° C. The solid weighed 57.4 grams after drying. It was a ring-opened 2-norbornene/1-butene copolymer having a DSV of about 2.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04136248
Source datasetuspto-grants-1979_01
ORD IDord-5761063912194cd2af00e6a1c6c2c493
Source noteuspto-grants-1979_01