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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1759980생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4,6-DichloropyrimidineHCID 70943—
반응물1-(Bromomethyl)-2,3-difluoro-benzeneHCID 517984—
반응물TmsciHCID 131723440—
촉매1,1-DibromoethaneHCID 11201—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-6-(2,3-difluorobenzyl)pyrimidineHCID 2259975238.4%

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 2.1 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06838463B2
출처 데이터셋uspto-grants-2005_01
ORD IDord-407976205e1f4b29b14d403fbc8ad084
출처 메모uspto-grants-2005_01