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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1592266생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1592266

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4,6-DichloropyrimidineHCID 70943—
반응물6-Chloro-2-fluoro-3-methylbenzyl bromideHCID 2773680—
반응물TmsciHCID 131723440—
촉매1,1-DibromoethaneHCID 11201—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-6-(2-chloro-5-methyl-6-fluorobenzyl)pyrimidineHCID 2259967219.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07291730B2
출처 데이터셋uspto-grants-2007_11
ORD IDord-98b37064430d4955a362251192d476e9
출처 메모uspto-grants-2007_11