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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2301333Erstellt: 26. Oktober 2026

Ammonia → 4-tert-Butyl-3,6-dichloropyridazine

https://huagongshe.com/reaction/2301333

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktSulfuric AcidHCID 1118—
EduktPivalic acidHCID 6417—
EduktAmmonium PersulfateHCID 62648—
Edukt3,6-DichloropyridazineHCID 67331—
KatalysatorSilver NitrateHCID 24470—
LösungsmittelWaterHCID 962—
Produkt4-tert-Butyl-3,6-dichloropyridazineHCID 8984653,5%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Concentrated sulfuric acid (53.6 ml, 1.0 mol) was added carefully to a stirred suspension of 3,6-dichloropyridazine (50.0 g, 0.34 mol) in water (1.25 l). This mixture was then heated to 70° C. (internal temperature) before the addition of trimethylacetic acid (47.5 ml, 0.41 mol). A solution of silver nitrate (11.4 g, 0.07 mol) in water (20 ml) was then added over approximately one minute. This caused the reaction mixture to become milky in appearance. A solution of ammonium persulphate (230 g, 1.0 mol) in water (0.63 l) was then added over 20-30 minutes. The internal temperature rose to approximately 85° C. During the addition the product formed as a sticky precipitate. Upon complete addition the reaction was stirred for an additional 10 minutes, then allowed to cool to room temperature. The mixture was then poured onto ice and basified with concentrated aqueous ammonia, with the addition of more ice as required to keep the temperature below 10° C. The aqueous was extracted with dichloromethane (3×300 ml). The combined extracts were dried (MgSO4), filtered and evaporated to give 55.8 g of crude product as an oil. This was purified by silica gel chromatography using 0-15% ethyl acetate in hexane as eluent to give 37.31 g (53%) of the desired compound. Data for the title compound: 1H NMR (360 MHz, d6-DMSO) δ1.50 (9H, s), 7.48 (1H, s); MS (ES+) m/e 205 [MH]+, 207 [MH]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06500828B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-426dbea02f744f5cab0421552fb5ae24
Quellennotizuspto-grants-2002_12