HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Acetylphenanthrene → 3-Phenanthrenecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Acetylphenanthrene | HCID 74867 | — |
| Reactant | Methyl 2-phenanthryl ketone | HCID 80060 | — |
| Reactant | Phenanthrene-2-carbaldehyde | HCID 3015327 | — |
| Product | 3-Phenanthrenecarboxylic acid | HCID 24056 | 51% |
Reaction Steps
Using the procedure outlined in 2A for 2-acetylphenanthrene, 3-acetylphenanthrene (Aldrich, technical grade), 25 g, 0.114 mol) gave 13 g (51%) of phenanthrene-3-carboxylic acid. 15.6 g (0.07 mol) of this acid was converted to the corresponding acid chloride, then to 8.37 g (58%) of phenanthrene-3-carboxaldehyde mp 78°-80° (lit. 79.5°-80°, E. Mosettig and J. van de Kamp, J. Amer. Chem. Soc. 55 2395 (1933)), (C, H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808625 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-51e3744d5edb47bb947311dfaff957f1 |
| Source note | uspto-grants-1989_02 |