HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-azido-6-methoxy-2,2-dimethyl-3,4-dihydronaphthalen-1(2H)-one → 4-amino-6-methoxy-2,2-dimethyl-3,4-dihydronaphthalen-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-azido-6-methoxy-2,2-dimethyl-3,4-dihydronaphthalen-1(2H)-one | HCID 86614023 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-amino-6-methoxy-2,2-dimethyl-3,4-dihydronaphthalen-1(2H)-one | HCID 66844958 | 91.2% |
Reaction Steps
To a solution of 4-azido-6-methoxy-2,2-dimethyl-3,4-dihydronaphthalen-1(2H)-one (2.50 g, 10.2 mmol) in EtOH (100 mL) at RT was added palladium on carbon (1.08 g, 10.2 mmol) in two portions. A hydrogen balloon was affixed to the reaction flask and the head space above the solvent was purged with H2. After 5 hours, the solution was filtered through a plug of celite and concentrated to provide the crude product as an oil. The residue was purified by column chromatography 100% DCM to 50% (10% MeOH/DCM/1% NH4OH) to provide the title compound as a yellow oil (2.04 g, 91% yield). MS m/z: 220.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872009B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-75a060ba9f81472db217a3bcacb2c640 |
| Source note | uspto-grants-2011_01 |