HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Ethyl(4-amino-2,3,5,6-tetrafluorobenzoyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | Ethyl (pentafluorobenzoyl)acetate | HCID 2760255 | — |
| Reactant | 2-(2,3,5,6-Tetrafluorophenyl)acetic acid | HCID 20536491 | — |
| Reactant | 4-Amino-2,3,5,6-tetrafluorophenylacetic acid | HCID 20536502 | — |
| Product | Ethyl(4-amino-2,3,5,6-tetrafluorobenzoyl)acetate | HCID 20536547 | — |
Reaction Steps
The [4-amino(mono- or poly-fluoro)phenyl]alkanoic acids and esters required as intermediates are prepared by a sequence of reactions involving nitration of a suitable phenylalkanoic acid followed by reduction of the nitro group. For example, 2,3,5,6-tetrafluorophenylacetic acid is converted to 4-amino-2,3,5,6-tetrafluorophenylacetic acid by this method. The [4-amino-(mono- or poly-fluoro)benzoyl]alkanoic acids and esters are prepared by the reaction of ammonia or sodium amide with (4-halobenzoyl)alkanoic acids. For example, the reaction of sodium amide with ethyl 2,3,4,5,6-pentafluorobenzoylacetate yields ethyl(4-amino-2,3,5,6-tetrafluorobenzoyl)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04333940 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-44759f576f0e49e699f30aa3e91ca86e |
| Source note | uspto-grants-1982_06 |