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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1717491Erstellt: 26. Oktober 2026

Triethylamine → 4-Cyano-3-fluorobenzyl methanesulfonate

https://huagongshe.com/reaction/1717491

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2-Fluoro-4-(hydroxymethyl)benzonitrileHCID 11829631—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Cyano-3-fluorobenzyl methanesulfonateHCID 21904620—

Reaktionsschritte

2-Fluoro-4-hydroxymethylbenzonitrile (1.3 g, 8.6 mmol; see step (ii) above) was dissolved in 50 mL of CH2Cl2 and cooled on an ice bath. Triethylamine (0.87 g, 8.6 mmol) and methanesulfonyl chloride (0.99 g, 8.7 mmol) were added. After stirring for 1.5 h the reaction mixture washed with 1M HCl. The organic phase was dried (Na2SO4) and evaporated. The product could be used without purification. Yield of a colourless oil: 1.8 g (92%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07803954B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-88a93786023543c29600724716f84d45
Quellennotizuspto-grants-2010_09