1-Hexene → HCID 86736255, compound

2500 ml dry toluene cosolvent, 350 ml 5,6-dimethyl-2-norbornene, 20 ml 1-hexene solution, and 45 ml diethylaluminum iodide solution were charged to a dry, nitrogen-purged glass gallon reactor. 56 ml of the MoCl5 solution was charged last with shaking. After 1.5 hours the reaction was shortstopped using a mixture of 5 ml ethanolamine, 15 ml Solution A, 60 ml of an antioxidant solution (0.1 g/ml of 2,2'-methylenebis-[4-methyl-6-t-butylphenol] in toluene), and 100 ml toluene. The polymer cement was coagulated batch-wise in a Waring blender using excess Solution A. 270 grams of a solid, ring-opened 5,6-dimethyl-2-norbornene/1-hexene copolymer was recovered after being filtered and vacuum dried at 60° C.

1. custompurged glass gallon reactor
2. addition56 ml of the MoCl5 solution was charged last
3. additiona mixture of 5 ml ethanolamine, 15 ml Solution A, 60 ml of an antioxidant solution (0.1 g/ml of 2,2'-methylenebis-[4-methyl-6-t-butylphenol] in toluene), and 100 ml toluene
4. custom270 grams of a solid, ring-opened 5,6-dimethyl-2-norbornene/1-hexene copolymer was recovered
5. filtrationafter being filtered
6. customvacuum dried at 60° C.

ORD record

ord-63588c0eee174503b10c5116817b3e8c

Source dataset

uspto-grants-1979_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04136247