HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-1-naphthol → 5-methoxynaphthalen-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-1-naphthol | HCID 65746 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-methoxynaphthalen-1-amine | HCID 235548 | 63% |
Reaction Steps
To a mixture of 10 g of 5-amino-1-hydroxynaphthalene in 250 ml of acetonitrile and 25 ml of methanol was added 15 ml of diisopropylethylamine followed by 44 ml of 2M TMSCHN2 in ether. The mixture was stirred at room temperature for 3.5 h after which it was concentrated to a dark oil. The material was purified by flash chromatography on silica gel, eluting with ethyl acetate/dichloromethane/heptane to provide 6.9 g (63%) of 5-amino-1-methoxynaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919628B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-06bcd6c8742a488ebc16f065a5fbaeef |
| Source note | uspto-grants-2011_04 |