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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 85178Erstellt: 23. Oktober 2026

Hydrochloric Acid → 3-(2,6-Dimethylmorpholino)benzaldehyde

https://huagongshe.com/de/reaction/85178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
Edukt2,6-DimethylmorpholineHCID 110862—
Edukt2-(3-Bromophenyl)-1,3-dioxaneHCID 10105815—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt3-(2,6-Dimethylmorpholino)benzaldehydeHCID 7673943875,4%

Reaktionsschritte

A mixture containing 2-(3-bromophenyl)-1,3-dioxane (136; 2.0 g, 8.23 mmol), 2,6-dimethylmorpholine (122; 1.14 g, 9.88 mmol), Pd2(dba)3 (50 mg), NaOt-Bu (1.39 g, 14.0 mmol) and BINAP (100 mg) in 20 mL of toluene was stirred at reflux for 5 h. Upon cooling to room temperature, enough cold 1N HCl (50 mL) was added to adjust the pH The resulting reaction mixture was stirred at room temperature for 1 h. NaOH(aq) was added to adjust the pH=11. The aqueous mixture was extracted with CH2Cl2 (3×50 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. Purification by chromatography (petroleum ether:EtOAc=10:1) afforded 3-(2,6-dimethylmorpholino)benzaldehyde 137 as a yellow oil (1.36 g, yield: 72%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846947B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-246fa3323393435ca51916887adbf9e1
Quellennotizuspto-grants-2014_09