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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 363190Erstellt: 26. Oktober 2026

Ammonium Hydroxide → 2-(3-Trifluoromethoxyphenyl)-5-methylpyridine

https://huagongshe.com/reaction/363190

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium HydroxideHCID 14923—
Edukt1-Bromo-3-(trifluoromethoxy)benzeneHCID 519964—
Edukt2-Bromo-5-methylpyridineHCID 564216—
EduktHCID 178418306HCID 178418306—
KatalysatorZincchlorideHCID 3007855—
KatalysatorNickel--triphenylphosphane (1/2)HCID 57357981—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelPentaneHCID 8003—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3-Trifluoromethoxyphenyl)-5-methylpyridineHCID 54520146—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 3-bromotrifluoromethoxybenzene (0.590 mL, 4.00 mmol) in THF (12 mL) at -78° C. was added t-butyl lithium (4.71 mL, of a 1.7M solution in pentane, 8.00 mmol. After 10 minutes zinc chloride(4.0 mL, of a 1M solution in diethylether, 4.00 mmol) was added. The reaction was stirred for 10 minutes at -78° C. and then allowed to warm to 0° C. and stirred for 30 minutes. This solution was added via cannula to a solution of 2-bromo-5-methyl pyridine and bis(triphenylphosphine) Nickel II chloride. The reaction stirred for 1 hour at 0° C. and then at ambient temperature for a furthur 1 hour. Saturated ammonium hydroxide solution (3 mL) was added and the mixture stirred until homogenous, extracted with Et2O and the organic extracts washed with saturated brine, dried (MgSO4) and evaporated in vacuo. The residue was chromatographed (Silica gel, 25-50% CH2Cl2 in hexanes).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05872136
Quelldatensatzuspto-grants-1999_02
ORD IDord-89439644dad44269915f26bafa0e3617
Quellennotizuspto-grants-1999_02