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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 478290Erstellt: 25. Oktober 2026

Potassium Carbonate → 3-Amino-4-chlorobenzaldehyde

https://huagongshe.com/reaction/478290

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktSodium DithioniteHCID 24489—
Edukt4-Chloro-3-nitrobenzaldehydeHCID 85505—
Katalysator1,1'-Diheptyl-4,4'-bipyridinium dibromideHCID 80262—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Amino-4-chlorobenzaldehydeHCID 245303102,4%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

4-Chloro-3-nitrobenzaldehyde (4.00 mg, 21.6 mmol) in CH2Cl2 (150 mL) at 23° C. was treated with water (50 mL) and N, N′-diheptyl-4,4′-bipyridinium dibromide (220 mg, 10 mg/mmol of substrate). The biphasic mixture was cooled to 5° C. and treated with a solution of sodium dithionite (15.0 g, 86.0 mmol) and K2CO3 (13.4 g, 87.0 mmol) in water (45 mL). The cooling bath was removed and the biphasic mixture stirred vigorously at 23° C. for 4 hours. The mixture was partitioned between additonal CH2Cl2 (75 mL) and water (50 mL) and the aqueous layer was extracted with CH2Cl2 (75 mL). The organic portions were washed with brine (75 mL) and dried (Na2SO4). The residue was treated with ethyl acetate (25 mL) and silica gel (75 g) and the suspension was filtered through a small pad of Celite, rinsing with 10% ethyl acetate/CH2Cl2 (15 mL). The filtrate was concentrated to provide the title compound as an off-yellow powder (3.44 g, 22%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06642222B2
Quelldatensatzuspto-grants-2003_11
ORD IDord-c2a40575cb554cf5aedc4426b7883632
Quellennotizuspto-grants-2003_11