HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acenaphthene → Acenaphthylene, dodecahydro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acenaphthene | HCID 6734 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Product | Acenaphthylene, dodecahydro- | HCID 102215 | 100% |
Reaction Steps
Acenaphthene was hydrogenated by the same procedure as in Example 4 except that the catalyst was replaced by a 5% Rh/C catalyst and reaction was effected at 150° C. for 30 minutes. Perhydroacenaphthene was produced in a yield of 100%, containing 1.1% of No. 1 isomer, 3.6% of No. 2 isomer, and 4.4% of No. 3 isomer, indicating a selectivity of No. 4 isomer of 90.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04783565 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-be6d29ca0ef3479797b3f28ae27053c0 |
| Source note | uspto-grants-1988_11 |