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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1664422Erstellt: 26. Oktober 2026

Ether, bis(1-chloroethyl) → 6-Chloro-5-methoxymethoxy-nicotinonitrile

https://huagongshe.com/reaction/1664422

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEther, bis(1-chloroethyl)HCID 23419—
EduktDiisopropylethylamineHCID 81531—
Edukt6-Chloro-5-hydroxynicotinonitrileHCID 86636455—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-Chloro-5-methoxymethoxy-nicotinonitrileHCID 8663645650%

Reaktionsschritte

To a solution of 6-chloro-5-hydroxy-nicotinonitrile (1.12 g, 7.24 mmol) in DCM (15 mL) was added N,N-diisopropyl ethylamine (1.57 mL, 9.05 mmol) followed by the addition of chloro-methyl methylether (0.66 mL, 8.69 mmol) slowly at 0° C. After overnight at room temperature, the reaction mixture was washed with saturated NaHCO3 (10 mL) and brine (10 mL), dried over Na2SO4, filtered, and concentrated to give yellow oil. Purification was accomplished by flash chromatography on silica gel using 5-25% EtOAc/hexanes gradient elution to yield the title compound (0.68 g, 50%) as a transparent oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.53 (d, J=2.0 Hz, 1H), 8.14 (d, J=2.0 Hz, 1H), 5.42 (s, 2H), 3.40 (s, 3H); MS (ES) m/z: 199 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08039450B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-5b118c597f9b40d8a5a20ee0830a0464
Quellennotizuspto-grants-2011_10