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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2209464Erstellt: 26. Oktober 2026

Methanol → HCID 54509567, Verbindung

https://huagongshe.com/reaction/2209464

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt3-Nitrophenylboronic AcidHCID 1677—
EduktSodium CarbonateHCID 10340—
Edukt2-bromo-4-(4-pyridinylmethyl)BenzenamineHCID 21865645—
LösungsmittelBenzeneHCID 241—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelAluminumHCID 5359268—
ProduktHCID 54509567HCID 5450956785,3%

Reaktionsschritte

4-(4-Amino-3-bromobenzyl)pyridine (1.0 gm), 3-nitrobenzene boronic acid (0.63 gm), palladium tetrakis triphenylphosphine (0.47 gm), methanol (6.5 mL), 2.0M Na2CO3 (1.9 mL) and benzene (32 mL) are combined in a reaction flask that is wrapped in aluminum foil (to prevent exposure of the reagents to light). The reaction mixture is heated to reflux for 6 hours. The progress of the reaction is monitored by thin-layer chromatography (9:1 hexane:ethyl acetate). When the starting material is converted, the reaction mixture is allowed to cool and the solvents are removed. Ethyl acetate is added to the residue, the resultant solution is filtered through a pad of Na2SO4, and concentrated. The product is isolated by preparative thin-layer chromatography (9:1 hexane:ethyl acetate) yielding 983 mg of 4-[4-amino-3-(3-nitrophenyl)benzyl]pyridine as an orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05455252
Quelldatensatzuspto-grants-1995_10
ORD IDord-81a3102cb48e4c0b8237898f90eb372f
Quellennotizuspto-grants-1995_10