HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylcyclohexane → Isobutylene 1,3,5-hexatriene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylcyclohexane | HCID 7962 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Ethylaluminum dichloride | HCID 11237 | — |
| Reactant | 1,3,5-Hexatriene | HCID 16695 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isobutylene 1,3,5-hexatriene | HCID 86737908 | — |
Reaction Steps
Operating with a reactor modified with respect to that used for the synthesis of POL 1, 2, 3 and 4, an isobutylene-1,3,5-hexatriene copolymer of low molecular weight was synthesised. 60 cm3 of methycyclohexane, 20 cm3 of methylene chloride, 28.4 g of isobutylene and 0.9 g of 1,3,5-hexatriene were fed, and the reaction was carried out at -10° C. 0.8 moles of AlEtCl2 were then introduced, and the mixture polymerised for fifteen minutes. 8.8 g of copolymer were isolated having a molecular weight of 10,000 and a conjugated unsaturation content of 0.38 moles/kg. By reaction with maleic anhydride, a functionalised polymer was obtained with 0.38 moles/kg of anhydride groups.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282337 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-98ab83bd827743f5b2034377e61bce34 |
| Source note | uspto-grants-1981_08 |