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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51968Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Amino-4-chlorobenzaldehyde

https://huagongshe.com/de/reaction/51968

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
Edukt4-Chloro-2-nitrobenzaldehydeHCID 79674—
KatalysatorIronHCID 23925—
LösungsmittelWaterHCID 962—
Produkt2-Amino-4-chlorobenzaldehydeHCID 1125213883%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a 3-neck flask fitted with a reflux condenser and a mechanical stirrer, were added 4-chloro-2-nitrobenzaldehyde (25 g, 135 mmol, 1 equiv), ethanol (375 mL), and water (100 mL). 4-Chloro-2-nitrobenzaldehyde can be obtained from P.H.T. International, Inc., Charlotte, N.C. Iron dust (225 mesh, Aldrich, Milwaukee, Wis.) (22.6 g, 405 mmol, 3 equiv) and concentrated hydrochloric acid (5.7 mL, 67.5 mmol, 0.5 equiv) was added. The slurry was heated to 85° C. for two hours, cooled to room temperature, filtered through diatomaceous earth and rinsed with ethanol (100 mL) and toluene (100 mL). The solution was transferred to a separatory funnel and toluene (300 mL) were added. The organic layer was washed with saturated sodium bicarbonate solution (300 mL) and brine (300 mL), then dried over sodium sulfate and then concentrated to provide 4-chloro-2-aminobenzaldehyde (17.4 g, 83%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713489B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-c8dc524c9eca4319a7070e985f4b955f
Quellennotizuspto-grants-2004_03