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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 587782Erstellt: 25. Oktober 2026

Ammonia → 4-Bromo-3,5-dichlorobenzaldehyde

https://huagongshe.com/reaction/587782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktTert-Butyl nitriteHCID 10906—
EduktMethyl 4-amino-3,5-dichlorobenzoateHCID 604808—
Edukt4-Bromo-3,5-dichloro-benzoic acid methyl esterHCID 50849686—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-Bromo-3,5-dichlorobenzaldehydeHCID 22421097—

Reaktionsschritte

Methyl 4-bromo-3,5-dichlorobenzoate: CuBr2 (7.5 g, 34.08 mmol) in MeCN (50 mL) was stirred at 80° C. for 30 min. To this solution tert-butylnitrite (6.5 mL, 54.55 mmol) was added dropwise at the same temperature and the mixture was stirred for another 10 min. Methyl 4-amino-3,5-dichlorobenzoate in MeCN (30 mL) was added dropwise to the reaction mixture which was then stirred at 80° C. for 30 min. The reaction mixture was brought to ambient temperature. Aqueous ammonia solution (20 mL) was added and extracted with petroleum ether. The organic layer was washed with brine followed by water. The organic solution was dried (Na2SO4), filtered and concentrated to afford the title compound as an off white solid (7.5 g, 77%): 1H NMR (300 MHz, DMSO-d6) δ 8.02 (s, 2H), 3.94 (s, 3H); ESIMS m/z 282 ([M]+); IR (thin film) 1733, 762, 514 cm−1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09226501B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-c5bd742776c54ec0a7ffe5bcc619d108
Quellennotizuspto-grants-2016_01