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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 927109Erstellt: 26. Oktober 2026

1-(Chloromethyl)-3,5-bis(trifluoromethyl)benzene → 3,4-bis(Benzyloxy)-6-{[3,5-bis(trifluoromethyl)phenyl]-methyl}pyridazine

https://huagongshe.com/reaction/927109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Chloromethyl)-3,5-bis(trifluoromethyl)benzeneHCID 123576—
EduktLithium ChlorideHCID 433294—
EduktMagnesiumHCID 5462224—
Edukt2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Edukt3,4-Bis(benzyloxy)-6-chloropyridazineHCID 12213474—
KatalysatorZincHCID 23994—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3,4-bis(Benzyloxy)-6-{[3,5-bis(trifluoromethyl)phenyl]-methyl}pyridazineHCID 8667703033%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a solution of 3,4-bis(benzyloxy)-6-chloropyridazine (Intermediate 1) (1 g, 3.06 mmol)dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.143 g, 0.3 mmol) and palladium (II) acetate (0.034 g, 0.15 mmol) in tetrahydrofuran (10 ml) under nitrogen was added the supernatant zinc reagent [generated from the addition of 1-(chloromethyl)-3,5-bis(trifluoromethyl)benzene (3 g, 11.43 mmol) to a suspension of magnesium (0.694 g, 28.6 mmol) in lithium chloride (28.6 ml, 14.28 mmol) in tetrahydrofuran (1M) and zinc(II) chloride (12.57 ml, 12.57 mmol) in tetrahydrofuran, warmed to 30° C. to initiate and stirred for one hour to complete] and the resulting red/brown mixture was heated at 65° C. for 16 hours. The reaction mixture was cooled, diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate solution, saturated aqueous ammonium chloride solution and brine. The organics were dried (MgSO4), filtered and solvent removed in vacuo to give a brown oil. The oil was purified by silica chromatography eluting with 0-40% ethyl acetate in petrol to yield the title compound (520 mg 33%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09290456B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-7419e22dd563442d9aeb0827d96f65fa
Quellennotizuspto-grants-2016_03