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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28376Erstellt: 24. Oktober 2026

Trimethylsilyl cyanide → 3-Chloro-2-cyano-2-(2-hydroxyethoxy)propyl acetate

https://huagongshe.com/de/reaction/28376

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilyl cyanideHCID 82115—
Edukt(2-(Chloromethyl)-1,3-dioxolan-2-yl)methyl acetateHCID 57426437—
Katalysatorzinc(II)iodideHCID 9883512—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Chloro-2-cyano-2-(2-hydroxyethoxy)propyl acetateHCID 57426438—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A mixture of (2-(chloromethyl)-1,3-dioxolan-2-yl)methyl acetate (67.8 mmol), trimethylsilyl cyanide (20.29 g, 204 mmol, TCI America) and zinc iodide (3.65 g, 11.4 mmol) was heated (40° C., oil bath) for 6 hrs, then at ambient temperature for 16 hrs. The mixture was diluted with CH2Cl2 (100 mL) and stirred with silica gel (50 g) for several hours. The mixture was loaded onto a flash silica gel column (350 g silica) and eluted with CH2Cl2 then increasing amounts of Et2O to a final eluent of 30% Et2O in CH2Cl2. Product fractions were pooled and concentrated in-vacuo to give the title compound as an amber oil: 1H NMR (500 MHz, CDCl3) δ ppm 4.44 (1H, d, J=-11.90 Hz), 4.35 (1H, d, J=11.90 Hz), 3.83-3.88 (2H, m), 3.79-3.84 (4H, m), 2.13-2.16 (3H, m); LC/MS m/z 222.16 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419969B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-99a368140e46451989d82193f02a1eef
Quellennotizuspto-grants-2008_09