HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dinitroadamantane → Adamantane-1,3-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dinitroadamantane | HCID 583950 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | Adamantane-1,3-diamine | HCID 213512 | 95% |
Reaction Steps
To an autoclave, 10 mmole of 1,3-dinitroadamantane obtained by the method of Example 16, 5% Pd-C (10 mole % of Pd relative to a substrate), 1 ml of dilute hydrochloric acid and 10 ml of methanol were charged. The mixture was stirred for 2 hours at 80° C. in an atmosphere of hydrogen at 30 atm. As a result, the conversion of 1,3-dinitroadamantane was 99%, and 1,3-diaminoadamantane (yield 95%) was formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06468487B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-259adce233294778a3db16244fbbbe09 |
| Source note | uspto-grants-2002_10 |