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HRID 7715Erstellt: 23. Oktober 2026

Ethyl Acetate → [4-(1,3-Benzoxazol-2-yl)-2-(methoxymethoxy)phenyl]acetonitrile

https://huagongshe.com/de/reaction/7715

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium CyanideHCID 8929—
Edukt2-[4-(Bromomethyl)-3-(methoxymethoxy)phenyl]-1,3-benzoxazoleHCID 21990942—
LösungsmittelN,N-Dimethylformamide--water (1/1)HCID 21962138—
Produkt[4-(1,3-Benzoxazol-2-yl)-2-(methoxymethoxy)phenyl]acetonitrileHCID 21990994—

Reaktionsschritte

2-[4-(Bromomethyl)-3-(methoxymethoxy)phenyl]-1,3-benzoxazole (250 mg, 0.72 mmol) was treated with sodium cyanide (150 mg, 2.2 mmol) in DMF/H2O (15 mL/1.5 mL) at 90° C. for 3 h and EtOAc (150 mL) was added. The EtOAc solution was washed with H2O (2×20 mL), brine (2×20 mL), dried (MgSO4), filtered, and concentrated in vacuo. The residue was eluted with flash column (silica gel, hexanes:EtOAc 4:1) to afford the desired [4-(1,3-benzoxazol-2-yl)-2-(methoxymethoxy)phenyl]acetonitrile as a yellow solid. 1H NMR (CD3OD, 300 MHz), δ 8.02 (d, 2H), 7.95 (m, 1H), 7.80 (m, 1H), 7.63 (m, 1H), 7.57 (d, 2H), 7.40 (m, 2H). MS (ESI) 295 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087601B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-1bb2abbd51504100ae8fddcf2916a41c
Quellennotizuspto-grants-2006_08