HuagongsheHuagongshe Chemistry Print Report · For research reference only
Selenium Dioxide → 1,2-Naphthoquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 2-Methyl-2,6,7,8-tetrahydro-chromen-5-one | HCID 11557341 | — |
| Reactant | Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate | HCID 12284900 | — |
| Product | 1,2-Naphthoquinone | HCID 10667 | — |
| Product | 5,6-Dioxo-5,6-dihydro-naphthalene-1-carboxylic acid methyl ester | HCID 9813198 | — |
| Product | Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate | HCID 12284900 | — |
Reaction Steps
Methyl 5-oxo-5,6,7,8-tetrahydro-1-naphthoate was prepared according to the literature (J. Org. Chem. 1976, p2918) from 2-methyl-2,6,7,8-tetrahydro-chromen-5-one (Tetrahedron Letters, 1975, p3407). Treatment of methyl 5-oxo-5,6,7,8-tetrahydro-1-naphthoate with selenium dioxide as described in Reference Example 1A yielded the corresponding 1,2-naphthoquinone, 5,6-dioxo-5,6-dihydro-naphthalene-1-carboxylic acid methyl ester, which was coupled with 2,3-diamino-benzoic acid, diacetate salt, as described in Reference Example 1A to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132419B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-f9a514ff147742fc9893084408fcf88e |
| Source note | uspto-grants-2006_11 |