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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 571791Erstellt: 25. Oktober 2026

Picolinic acid → HCID 66653709, Verbindung

https://huagongshe.com/reaction/571791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPicolinic acidHCID 1018—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2,3-DimethyliodobenzeneHCID 141645—
EduktHCID 66654239HCID 66654239—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktHCID 66653709HCID 66653709—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a degassed solution of 2-(4-hydroxy-phenyl)-morpholine-4-carboxylic acid tert-butyl ester (10.23 g; 36.6 mmol), and 1-iodo-2,3-dimethyl-benzene (10.62 g; 45.8 mmol) in DMSO (50 mL), was added picolinic acid (0.90 g; 7.3 mmol), CuI (0.70 g; 3.7 mmol) and K3PO4 (15.55 g; 73.3 mmol). The resulting mixture was heated overnight, at 90° C. After cooling to RT, brine was added and the mixture extracted with CH2Cl2. The combined organic layers were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (SiO2, CH2Cl2) to afford 2-[4-(2,3-dimethyl-phenoxy)-phenyl]-morpholine-4-carboxylic acid tert-butyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09029371B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-d646cfaf2d234009a22bae0a8e0e0f5d
Quellennotizuspto-grants-2015_05