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HRID 474713作成日:2026年10月24日

methyl (2E)-3-[2-(trifluoromethyl)-5-pyrimidinyl]-2-propenoate → Methyl 3-[2-(trifluoromethyl)-5-pyrimidinyl]propanoate

https://huagongshe.com/ja/reaction/474713

反応式

関与物質

役割名称HCID仕込み量
反応物methyl (2E)-3-[2-(trifluoromethyl)-5-pyrimidinyl]-2-propenoateHCID 21936364—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物Methyl 3-[2-(trifluoromethyl)-5-pyrimidinyl]propanoateHCID 2193621165.9%

反応手順

A mixture of methyl (2E)-3-[2-(trifluoromethyl)-5-pyrimidinyl]-2-propenoate (870 mg, 3.75 mmol) and Pd/C (39.9 mg, 0.375 mmol) in methanol (4 mL) was stirred at room temperature for 1 h under hydrogen. After cooling, the mixture was filtered through silica gel. The filtrate was concentrated to afford the title compound (577 mg, 2.47 mmol, 65.8% yield). LCMS: rt=2.47 min, [M+H+]=235

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637536B2
出典データセットuspto-grants-2014_01
ORD IDord-587bca349fe84a28b06b158480d5c30c
出典メモuspto-grants-2014_01