HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dimethyladamantane → 1-Ethyladamantane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dimethyladamantane | HCID 12800 | — |
| Reactant | Acenaphthylene, dodecahydro- | HCID 102215 | — |
| Product | 1-Ethyladamantane | HCID 522637 | — |
Reaction Steps
The same experiment as described in 2th line from the bottom in Table 5 of Example 5 was carried out except that perhydroacenaphthene prepared by hydrogenation of acenaphthene was used in place of TMN. Conversion rate of perhydroacenaphthene was 75.4%, and 1,3-dimethyladamantane and 1-ethyladamantane were obtained at 33.0% and 47.1% of selectivity and at 24.9% and 35.0% of yield respectively. Moreover, when amounts of catalyst was increased from 2 g to 4 g, conversion rate of perhydroacenaphthene was 85.6%, and 1,3-dimethyladamantane and 1-ethyladamantane were obtained at 45.2% and 6.6% of selectivity and at 38.7% and 5.7% of yield respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03944626 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-e1089c161b5944de91ab0aea965c0111 |
| Source note | uspto-grants-1976_03 |