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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1950628Erstellt: 26. Oktober 2026

(4-(Benzyloxy)phenyl)methanol → 4-Benzyloxybenzylamine

https://huagongshe.com/reaction/1950628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-(Benzyloxy)phenyl)methanolHCID 70043—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktP,P-Diphenylphosphinic azideHCID 199401—
LösungsmittelTolueneHCID 1140—
Produkt4-BenzyloxybenzylamineHCID 429284581%

Reaktionsschritte

To a solution of 4-benzyloxybenzyl alcohol (3.1 g) in toluene (40 ml) were sequentially added diphenylphosphoryl azide (4.8 g) and 1,8-diazabicyclo[5.4.0]undec-7-ene (2.6 g), and the solution was stirred for 25 hours at room temperature. The solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. Obtained by purifying the residue by silica gel column chromatography (hexane-ethyl acetate system), to a solution of the resulting 1-azidomethyl-4-benzyloxybenzene (3.0 g) in tetrahydrofuran (40 ml) were sequentially added water (3 ml) and triethylphosphine (2.0 ml), and the solution was stirred for 1 hour and 10 minutes at room temperature. The reaction solution was concentrated in vacuo, extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (2.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08399520B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-48e69354d10f44be8e082ccc009f4604
Quellennotizuspto-grants-2013_03