HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12070472, compound → HCID 12070473, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12070472 | HCID 12070472 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 12070473 | HCID 12070473 | 70% |
Reaction Steps
An autoclave was charged, 10 mmole of 1-acetyloxy-3-nitroadamantane obtained by the method of Example 14, 5% Pd-C (10 mole % of Pd relative to a substrate), 1 ml of dilute hydrochloric acid and 10 ml of methanol. 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-acetyloxy-3-nitroadamantane was 90%, and 1-acetyloxy-3-aminoadamantane (yield 70%) was formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392104B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-ceb98468216143f18a25c795d850d08e |
| Source note | uspto-grants-2002_05 |