戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1759980作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4,6-DichloropyrimidineHCID 70943—
反応物1-(Bromomethyl)-2,3-difluoro-benzeneHCID 517984—
反応物TmsciHCID 131723440—
触媒1,1-DibromoethaneHCID 11201—
触媒ZincHCID 23994—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-6-(2,3-difluorobenzyl)pyrimidineHCID 2259975238.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06838463B2
出典データセットuspto-grants-2005_01
ORD IDord-407976205e1f4b29b14d403fbc8ad084
出典メモuspto-grants-2005_01