HuagongsheHuagongshe Chemistry Print Report · For research reference only
Menadiol → 1,4-Naphthoquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Menadiol | HCID 10209 | — |
| Reactant | 1,4-Naphthalenediol | HCID 11305 | — |
| Product | 1,4-Naphthoquinone | HCID 8530 | 93% |
Reaction Steps
Using the same procedure, napthalene- 1,4-diol and 1,4-dihydroxy-2-methyl-naphthalene were oxidized to obtain a 93% yield of 1,4-naphthoquinone and a 97% yield of 2-methyl-1,4-naphthoquinone, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03941811 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-52f71c34f2f04ae1a9274cc5665b661b |
| Source note | uspto-grants-1976_03 |