Process for preparing arylalkanoic acid derivatives
US4142054A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Jun 16, 1977 |
| Grant date | Feb 27, 1979 |
| Priority date | — |
| Expiry date | Jun 16, 1997 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07C51/09
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
2-Aryl-C.sub.3 to C.sub.6 -alkanoate esters are prepared economically by reacting an enol ether of an aryl alkyl ketone with a trivalent thallium salt in an organic solvent. The trivalent thallium ions can be regenerated by adding a peracid and a reactive form of manganese, ruthenium, cobalt, iridium, hafnium, osmium or neobium to oxidize monovalent thallium ions to the trivalent state, in a sequential, continuous or stoichiometric procedure. A continuous process using a Scheibel column is disclosed. The ester intermediate product is then converted to the corresponding 2-aryl-C.sub.3 - to C.sub.6 -alkanoic acid or salt thereof. The aryl group is selected so the resulting acid product will be a useful compound such as an anti-inflammatory, analgesic and anti-pyretic drug or agriculturally useful product. Examples of drug acids which can be made by this process include ibuprofen, flurbiprofen, fenoprofen and naproxen and the like.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.