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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 547428Erstellt: 24. Oktober 2026

Triphenylphosphine → 4-(2-Morpholin-4-ylethoxy)benzeneboronic acid, pinacol ester

https://huagongshe.com/de/reaction/547428

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2-MorpholinoethanolHCID 61163—
Edukt4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734624—
EduktDiisopropyl azodicarboxylateHCID 5363146—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-Morpholin-4-ylethoxy)benzeneboronic acid, pinacol esterHCID 462591074%

Reaktionsschritte

To a stirring solution of 4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-phenol (2.55 g, 11.58 mmol), 2-morpholin-4-ylethanol (1.60 mL, 1.73 g, 13.2 mmol) and triphenyl phosphine (3.64 g, 13.9 mmol) in methylene chloride (60 mL) at 0° C. was added dropwise DIAD (2.82 g, 13.9 mmol). The reaction was allowed to warm to room temperature and stir overnight. After 18 hours, additional portions of triphenyl phosphine (1.51 g, 5.8 mmol), 2-morpholin-4-ylethanol (0.70 mL, 5.8 mmol), and DIAD (1.17 g, 5.8 mmol) were added. After stirring an additional 2 hours at room temperature the reaction was concentrated and the residue purified by flash chromatography (5% to 25% EtOAc in CHCl3) to provide the product as a white solid (2.855 g, 74%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07939529B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-660460debd8749d693ca32170a6fd42d
Quellennotizuspto-grants-2011_05