Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1617401Erstellt: 26. Oktober 2026

Benzoyl Peroxide → Ethyl 6-(bromomethyl)-2-(trifluoromethyl)pyrimidine-4-carboxylate

https://huagongshe.com/reaction/1617401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
EduktEthyl 6-methyl-2-(trifluoromethyl)pyrimidine-4-carboxylateHCID 67390769—
LösungsmittelCarbon TetrachlorideHCID 5943—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 6-(bromomethyl)-2-(trifluoromethyl)pyrimidine-4-carboxylateHCID 58431340—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of ethyl 6-methyl-2-(trifluoromethyl)pyrimidine-4-carboxylate (1.1 g, 4.5 mmol, prepared as described in WO 2007/090748), N-bromosuccinimide (2.86 g, 16.1 mmol) and benzoyl peroxide (0.21 g, 0.9 mmol) in carbon tetrachloride (9 mL) was heated in a sealed vessel to 100° C. overnight. The mixture was diluted with dichloromethane (DCM), filtered and the solvent was removed in vacuo. Purification via preparative HPLC-MS (C18 eluting with a gradient of MeCN/H2O containing 0.15% NH4OH) afforded the product, which on removal of solvent, was an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08765734B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-f728d6ece63f461a8adbc30112a9ffb4
Quellennotizuspto-grants-2014_07