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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1590375Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-Chloro-3-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/1590375

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAnilineHCID 6115—
EduktNitroneHCID 6350—
EduktSodium SulfiteHCID 24437—
Edukt4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
EduktSodium AcetateHCID 517045—
EduktFormaldehyde, oxime, hydrochloride (1:1)HCID 20257314—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
Produkt4-Chloro-3-(trifluoromethyl)benzaldehydeHCID 1186428,8%

Reaktionsschritte

To a suspension of 4-chloro-3-trifluoromethylaniline (ex Fluorochem) (15.9 g) in water (16 ml) was added concentrated hydrochloric acid (18 ml) Ice (30 g) was added and the mixture cooled to 0° and treated with sodium nitrite (5.6 g) in water (8 ml). After 15 minutes the mixture was made neutral to congo red with sodium acetate (8 g) in water (10 ml). A solution of formaldoxime, prepared from formaldoxime hydrochloride (ex Lancaster) (9.9 g) and sodium acetate (12 g) (ex BDH) in water (57 ml), at 10° was treated with cupric sulphate (2 g) (ex BDH) and sodium sulphite (0.34 g) followed by sodium acetate (55 g) in water (60 ml). The previously prepared mixture (from the aniline) was added dropwise at 10°-15°. After one hour at 15° hydrochloric acid (77 ml) was added and the mixture worked up in the usual manner. Purification by distillation (80°, 0.5 mmHg) gave 4-chloro-3-trifluoromethylbenzaldehyde (1.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05202356
Quelldatensatzuspto-grants-1993_04
ORD IDord-32d3f09eb68347d3a7734a4a7956c177
Quellennotizuspto-grants-1993_04