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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1759980Erstellt: 23. Oktober 2026

Water → 4-Chloro-6-(2,3-difluorobenzyl)pyrimidine

https://huagongshe.com/de/reaction/1759980

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4,6-DichloropyrimidineHCID 70943—
Edukt1-(Bromomethyl)-2,3-difluoro-benzeneHCID 517984—
EduktTmsciHCID 131723440—
Katalysator1,1-DibromoethaneHCID 11201—
KatalysatorZincHCID 23994—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Chloro-6-(2,3-difluorobenzyl)pyrimidineHCID 2259975238,4%

Reaktionsschritte

In 10 ml of tetrahydrofuran was suspended 1.3 g of zinc (powder), to which dibromoethane (2 drops) was added. The mixture was heated under reflux for 5 minutes, to which trimethylsilane chloride was added. The mixture was further heated under reflux for 5 minutes, to which a solution of 2.1 g of 2,3-difluorobenzyl bromide dissolved in 20 ml of tetrahydrofuran was slowly added with heating under reflux, followed by stirring for 20 minutes. (The solution thus obtained is referred to as solution G). In 10 ml of tetrahydrofuran were suspended 1.5 g of 4,6-dichloropyrimidine and 0.1 g of dichlorobistriphenylphosphine palladium, to which the above solution G was added, followed by heating under reflux for 3 hours and further stirring at room temperature for 12 hours. The reaction mixture was then poured into water and extracted three times with ethyl acetate. The organic layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.93 g of 4-chloro-6-(2,3-difluorobenzyl)pyrimidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06838463B2
Quelldatensatzuspto-grants-2005_01
ORD IDord-407976205e1f4b29b14d403fbc8ad084
Quellennotizuspto-grants-2005_01