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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704471Generated: October 26, 2026

Propionic Acid → Flumiclorac-pentyl

https://huagongshe.com/reaction/704471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic AcidHCID 1032—
ReactantTolueneHCID 1140—
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
Reactant4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)anilineHCID 14617850—
CatalystPiperidineHCID 8082—
SolventWaterHCID 962—
ProductFlumiclorac-pentylHCID 44304891.7%

Reaction Steps

A mixture of the compound (II) (12.0 g), 3,4,5,6-tetrahydrophthalic anhydride (7.56 g), piperidine (0.18 g), propionic acid (0.30 g) and toluene (24 g) was heated under reflux for 5 hours, during which water as by-produced was azeotropically removed. To the reaction mixture, toluene (24 g) and water (24 g) were added, and the organic layer was separated and concentrated under reduced pressure. To the residue, water (18 g) and methanol (33 g) were added, and the precipitated crystals were collected by filtration to give N-[4-chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)phenyl]-3,4,5,6-tetrahydrophthalimide (Compound (I)) (16.1 g). By the use of a high speed liquid chromatography, the purity of the compound (I) as the major product and the amount of the by-produced 4-chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)acetanilide (hereinafter referred to as "N-acetyl compound") as a contaminant were determined according to the inner standard method and the area comparison method, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987247
Source datasetuspto-grants-1991_01
ORD IDord-3637325cad1343d794afc80ea7b2a3ca
Source noteuspto-grants-1991_01