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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 67804Erstellt: 23. Oktober 2026

Chloroacetic Acid → Trichlorophenoxyacetic acid

https://huagongshe.com/de/reaction/67804

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetic AcidHCID 300—
Edukt2,4,5-TrichlorophenolHCID 7271—
Edukt2,3,7,8-Tetrachlorodibenzo-P-DioxinHCID 15625—
ProduktTrichlorophenoxyacetic acidHCID 1480—

Reaktionsschritte

The above objects have been achieved by the synthesis of 2,4,5-trichlorophenoxyacetic acid and its intermediate, 2,4,5-trichlorophenol, which are free from contamination with 2,3,7,8-tetrachloro-dibenzo-p-dioxin (TCDD). The synthesis involves the nitration of 1,2,4-trichlorobenzene to form 1,2,4-trichloro-5-nitrobenzene, which is reduced (usually with hydrogen) to produce 2,4,5-trichloroaniline. The 2,4,5-trichloroaniline is reacted with sulfuric acid and a nitrite to form 2,4,5-trichlorobenzenediazonium sulfate, which is reacted with water and distilled to produce 2,4,5-trichlorophenol which is analytically free of TCDD. The 2,4,5-trichlorophenol is reacted with monochloroacetic acid in the presence of aqueous base, followed by acidification, to produce 2,4,5-trichlorophenoxyacetic acid which also is analytically free of TCDD.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04346248
Quelldatensatzuspto-grants-1982_08
ORD IDord-fba6f8598a6943259c880685fa46ed63
Quellennotizuspto-grants-1982_08