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HRID 397371作成日:2026年10月25日

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

https://huagongshe.com/reaction/397371

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl benzoateHCID 7165—
反応物4-Methyl-2-(methylsulfanyl)pyrimidineHCID 821261—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒TetrahydrofuranHCID 8028—
生成物2-[2-(Methylsulfanyl)pyrimidin-4-yl]-1-phenylethan-1-oneHCID 1298582999.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610697B1
出典データセットuspto-grants-2003_08
ORD IDord-6b5de7a632a44f69a9fe8f875b648dd4
出典メモuspto-grants-2003_08