HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adamantane → Decyl adamantane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adamantane | HCID 9238 | — |
| Reactant | 1-Decene | HCID 13381 | — |
| Reactant | Aluminum bromide | HCID 24409 | — |
| Catalyst | Aluminum bromide | HCID 24409 | — |
| Solvent | Dibromomethane | HCID 3024 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Decyl adamantane | HCID 22416186 | — |
Reaction Steps
Decyl adamantane was prepared by reacting 140 g 1-decene, 54.4 gram adamantane in 100 cc n-hexane solvent and using 3 mmoles 1.0M AlBr3 in CH2Br2 or AlBr3 catalyst at 15°-50° C. reaction temperature. The product was isolated by quench the catalyst with dilute acid and aqueous work-up followed by distillation at 155° C. and 0.2 mm-Hg using a Kugelrohr to remove any C20 -material. The C30 + fraction was obtained in 80% yeild. It was hydrogenated at 200° C. and 500 psi H2 using 1 wt. % Ni/SiO2 catalyst.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05400427 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-d49e72834c184b4ca802e6b211731842 |
| Source note | uspto-grants-1995_03 |