Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triglyme | HCID 8189 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,10-Decanediol | HCID 37153 | — |
| Reactant | HCID 123913288 | HCID 123913288 | — |
| Product | HCID 18757654 | HCID 18757654 | — |
Reaction Steps
In a one-liter three-necked flask fitted with a mechanical stirrer and a Soxhlet extractor packed with 3A molecular sieves (about 15 g) and topped with a condenser, 25.1 g of di-(n-decyl)cyclopentadiene (73 mmol), 12.6 g of 1,10-decanediol (73 mmol), 5 g of KOH, and 250 g of triglyme were stirred and deoxygenated with a stream of nitrogen. The mixture was then heated to reflux under nitrogen for two hours. The mixture was cooled and washed with water to remove base and triglyme. The product was dried and hydrogenated over palladium on carbon. The resulting product was characterized by gel permeation chromatography to determine the molecular weight. The number average molecular weight was 1250, indicating that on average about 3 di(n-decyl)cyclopentadienes had been crosslinked. The weight average molecular weight of 2250 indicates that molecules containing a higher number of crosslinked di(n-decyl)cyclopentadienes were formed. The measured viscosity at 100°, 40 cSt, is consistent with these high molecular weights.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07244522B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-854a69272cd848a981fb6acb164059c4 |
|---|
| Source note | uspto-grants-2007_07 |
|---|