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HRID 704471作成日:2026年10月25日

Propionic Acid → Flumiclorac-pentyl

https://huagongshe.com/reaction/704471

反応式

関与物質

役割名称HCID仕込み量
反応物Propionic AcidHCID 1032—
反応物TolueneHCID 1140—
反応物3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
反応物4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)anilineHCID 14617850—
触媒PiperidineHCID 8082—
溶媒WaterHCID 962—
生成物Flumiclorac-pentylHCID 44304891.7%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04987247
出典データセットuspto-grants-1991_01
ORD IDord-3637325cad1343d794afc80ea7b2a3ca
出典メモuspto-grants-1991_01