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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397371생성일: 2026년 10월 24일

Ethyl benzoate → 2-[2-(Methylsulfanyl)pyrimidin-4-yl]-1-phenylethan-1-one

https://huagongshe.com/ko/reaction/397371

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl benzoateHCID 7165—
반응물4-Methyl-2-(methylsulfanyl)pyrimidineHCID 821261—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
용매TetrahydrofuranHCID 8028—
생성물2-[2-(Methylsulfanyl)pyrimidin-4-yl]-1-phenylethan-1-oneHCID 1298582999.5%

반응 단계

86 ml (86 mmoles) of 1.0 M sodium bis(trimethylsilyl)amide in tetrahydrofuran was added drop-wise by addition funnel to a solution of 6.03 g (43 mmoles) 4-methyl-2-(methylthio)pyrimidine and 6.46 g (43 mmoles) ethyl benzoate in 86 ml tetrahydrofuran under a nitrogen atmosphere. After 2 hours the reaction was quenched with saturated ammonium chloride solution. Most of the tetrahydrofuran was removed in vacuo. The residue was diluted with 400 ml ethyl acetate and 200 ml water. The organic layer was separated and washed 2×100 ml saturated sodium chloride solution, separated, dried over Na2SO4, filtered, and concentrated in vacuo to give 10.45 g (42.77 mmoles) of 2-[2-(methyl thio)pyrimidin-4-yl]-1-phenyle thanone as a viscous red-brown oil that solidified upon standing. MH+=244.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610697B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-6b5de7a632a44f69a9fe8f875b648dd4
출처 메모uspto-grants-2003_08