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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 618471Erstellt: 24. Oktober 2026

Nitric Acid → 2-Nitro-5-(2-chloro-alpha,alpha,alpha-trifluoro-4-tolyloxy) benzoic acid

https://huagongshe.com/de/reaction/618471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
EduktSulfuric AcidHCID 1118—
EduktAcetic AnhydrideHCID 7918—
Edukt3-(2-Chloro-alpha,alpha,alpha-trifluoro-4-tolyloxy)-benzoic acidHCID 19828811—
LösungsmittelButyl AcetateHCID 31272—
Produkt2-Nitro-5-(2-chloro-alpha,alpha,alpha-trifluoro-4-tolyloxy) benzoic acidHCID 8674736785%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Acetic anhydride (37.7 g) was added to 3-(2-chloro-α,α,α-trifluoro-4-tolyloxy)-benzoic acid (86% strength, 45 g) in n-butyl acetate (85.8 g) at 35° C. Sulphuric acid (98%, 12.2 g) was added slowly and the mixture cooled to 0° C. Nitric acid (90%, 10.4 g) was then added slowly over about 3 hours such that the temperature was maintained at -5 to 0° C. On completion of the nitric acid addition the reaction was quenched with water (60 g) at 0° C. The mixture was warmed to 50-60° C. and the aqueous layer removed. The solvent layer was washed with water (2×100 g) at 60° C. and the aqueous layer removed. The solvent and acetic acid were removed by distillation to give 2-nitro-5-(2-chloro-α,α,α-trifluoro-4-tolyloxy) benzoic acid (85%), 2'-nitro isomer (7.5 to 8.5 pph), total dinitro's (~0.5 pph).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05952531
Quelldatensatzuspto-grants-1999_09
ORD IDord-08f7744ce4ec4e63976db311a0570b43
Quellennotizuspto-grants-1999_09