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HRID 51286Erstellt: 23. Oktober 2026

Nitrogen → 1,6-Bis[4-(3-hydroxypropyl)phenoxy]hexane

https://huagongshe.com/de/reaction/51286

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktPotassium CarbonateHCID 11430—
Edukt1,6-DiiodohexaneHCID 12373—
Edukt3-(4-Hydroxyphenyl)propanolHCID 82452—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt1,6-Bis[4-(3-hydroxypropyl)phenoxy]hexaneHCID 2195985965%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A solution of 3-(4-hydroxyphenyl)-1-propanol 35 (3.3 g, 21.7 mmole) and 1,6-di-iodohexane (3.5 g, 8.88 mmole) in dimethylsulfoxide (40 mL) was degassed and saturated with N2 gas and potassium carbonate (4.5 g, 32.56 mmole) was added. The reaction mixture was stirred at 80° C. for 18 h under nitrogen atmosphere and then quenched with brine (150 mL). The product was extracted with EtOAc (200 mL) and the organic extracts were washed with 0.1 M NaOH and brine, and dried with MgSO4. The organics were removed in vacuo to give a pale brown solid. The solid was purified by flash silica column chromatography: 4/1 hexane/EtOAc to 5% MeOH in 1/1 hexane/EtOAc to give 1,6-bis[4-(3-hydroxypropyl)phenoxy]hexane 36 (Rf=0.17 in 1/1 hexane/EtOAc) in 65% yield (2.23 g). 1H-NMR (CD3OD, 299.96 MHz): δ (ppm) 7.08-7.05 (d, 4H), 6.80-6.77 (d, 4H), 3.93-3.89 (t, 4H), 3.56-3.52 (t, 4H), 2.64-2.56 (t, 4H), 1.81-1.69 (m, 8H), 1.44-1.21 (m, 4H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713651B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-b4e770601f45454db6e4faf14ec4e779
Quellennotizuspto-grants-2004_03