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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 82942Erstellt: 24. Oktober 2026

Benzyl Bromide → 3-(Benzyloxy)-1-(diphenylmethyl)azetidine

https://huagongshe.com/de/reaction/82942

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktSodium hydrideHCID 24758—
Edukt1-(Diphenylmethyl)azetidin-3-olHCID 330448—
KatalysatorAcetic AcidHCID 176—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(Benzyloxy)-1-(diphenylmethyl)azetidineHCID 1608944824,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 1-diphenylmethylazetidin-3-ol (300 mg, 1.3 mmol) in DMF (2.6 mL) at 0° C. under nitrogen was added NaH (60% in oil, 56 mg, 1.4 mmol). The suspension was stirred for 0.5 h at 0° C. then treated with benzyl bromide (236 μL, 2.0 mmol). The mixture was allowed to warm to room temperature then heated to 80° C. overnight. The reaction mixture was cooled, acetic acid (20 drops) was added and the mixture concentrated under reduced pressure. The crude material was purified on column chromatography (eluent: Pentane/EtOAc, 95/5 to 70/30) to give the product (104 mg, 24%) as an orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846711B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-df8f8c4729084f1e89502c2b257a43f8
Quellennotizuspto-grants-2014_09