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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156094Generated: November 1, 2026

Ammonia → Ethyl(4-amino-2,3,5,6-tetrafluorobenzoyl)acetate

https://huagongshe.com/reaction/1156094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium amideHCID 24533—
ReactantEthyl (pentafluorobenzoyl)acetateHCID 2760255—
Reactant2-(2,3,5,6-Tetrafluorophenyl)acetic acidHCID 20536491—
Reactant4-Amino-2,3,5,6-tetrafluorophenylacetic acidHCID 20536502—
ProductEthyl(4-amino-2,3,5,6-tetrafluorobenzoyl)acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04333940
Source datasetuspto-grants-1982_06
ORD IDord-44759f576f0e49e699f30aa3e91ca86e
Source noteuspto-grants-1982_06