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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 712677Erstellt: 23. Oktober 2026

Morpholine → 4-(5-Bromopyridin-3-yl)morpholine

https://huagongshe.com/de/reaction/712677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
Edukt3,5-DibromopyridineHCID 69369—
EduktBinap, (A+-)-HCID 634876—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt4-(5-Bromopyridin-3-yl)morpholineHCID 4673961450,8%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

In a sealable tube, to a mixture of 3,5-dibromo-pyridine (3.3 g, 13.8 mmol) and NaOtBu (0.051 g, 23 mmol) in toluene (70 mL), is added morpholine (1.0 g, 11.5 mmol). The mixture is bubbled with Argon for 5 min, and then BINAP (428.9 mg, 0.69 mmol) and Pd2(dba)3 (210.2 mg, 0.23 mmol) are added. The reaction mixture is bubbled with Argon for another 5 min. Then the cap is sealed and the reaction mixture is heated at 120° C. overnight and then is cooled to room temperature. The reaction mixture is filtered through diatomaceous earth and washed with DCM. The filtrate is partitioned between water and DCM. The aqueous phase is further extracted with DCM (2×). The combined DCM phases are concentrated. The crude is purified by flash chromatography on a silica gel column (EtOAc/heptane 0 to 50% gradient, then 50%) to provide 1.42 g of 4-(5-bromo-3-pyridyl)morpholine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09181272B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-7a234e61718c4a5fb21caffcce39713f
Quellennotizuspto-grants-2015_11