HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxy-1,4-Naphthoquinone → 2-Methoxynaphthalene-1,4-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxy-1,4-Naphthoquinone | HCID 16871 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxynaphthalene-1,4-diol | HCID 12563544 | — |
Reaction Steps
A solution of 2-methoxy-1,4-naphthoquinone (20.0 g) in tetrahydrofuran (150 mL) was hydrogenated at atmospheric pressure over Pd-C (10%, 0.5 g) until the calculated amount of hydrogen was absorbed, approximately 4 hours. Filtering off the catalyst under an atmosphere of nitrogen gave a solution of the desired product, which was used as such without isolation of the product as the starting material in Examples 1, 2 and 3, infra. Alternatively, the solvent is removed under reduced pressure and the residue recrystallized from diethyl ether/pentane, affording 2-methoxy-1,4-dihydroxynaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134161 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-20da1a44278c47c0ae2d9953ff17eaea |
| Source note | uspto-grants-1992_07 |