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HRID 1592266作成日:2026年10月27日

Water → 4-Chloro-6-(2-chloro-5-methyl-6-fluorobenzyl)pyrimidine

https://huagongshe.com/reaction/1592266

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6-Chloro-2-fluoro-3-methylbenzyl bromideHCID 2773680—
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-chloro-5-methyl-6-fluorobenzyl)pyrimidineHCID 2259967219.4%

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 2.4 g of 2-chloro-5-methyl-6-fluorobenzyl 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 0). 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 L 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 0.53 g of 4-chloro-6-(2-chloro-5-methyl-6-fluorobenzyl)pyrimidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07291730B2
出典データセットuspto-grants-2007_11
ORD IDord-98b37064430d4955a362251192d476e9
出典メモuspto-grants-2007_11