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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2167163Erstellt: 27. Oktober 2026

Triethylamine → 6-((di-tert-Butylphosphino)methyl)-2,2'-bipyridine

https://huagongshe.com/reaction/2167163

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPhosphine, bis(1,1-dimethylethyl)-HCID 136643—
Edukt2,2'-Bipyridine, 6-(chloromethyl)-HCID 642843—
LösungsmittelMethanolHCID 887—
Produkt6-((di-tert-Butylphosphino)methyl)-2,2'-bipyridineHCID 5323414685%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To an oven dried 50 mL pressure vessel equipped with magnetic stirring bar was added 6-chloromethyl-2,2′-bipyridine (BPy-CH2Cl) (2.05 g, 10.00 mmol), di-tert-butyl phosphine (1.75 g, 12.00 mmol), and 30 mL MeOH in a nitrogen glove box. The flask was sealed and heated at 50° C. for 48 hrs with stirring outside the glove box. After cooling, it was reintroduced to the glove box, triethylamine (1.82 g, 18.00 mmol) was added and the reaction mixture was stirred at room temperature for 1 hr. The solvents were removed under reduced pressure to obtain a white solid. The residue was washed with ether (3×20 mL) and the ether filtered and was removed under reduced pressure to yield a white solid. It was recrystallized from MeOH at ca. −30° C. to yield 2.67 g (85%) of 6-di-tert-butylphosphinomethyl-2,2′-bipyridine (BPy-tPNN).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09045381B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-b309024d2e2b451fbcb6027f7fc5c0a6
Quellennotizuspto-grants-2015_06