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HRID 715342作成日:2026年10月26日

Sodium Bicarbonate → Ethanone, 1-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]-

https://huagongshe.com/reaction/715342

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物N-methoxy-N-methyl-6-(2,2,2-trifluoroethoxy)pyridine-3-carboxamideHCID 86707284—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物Ethanone, 1-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]-HCID 5862912483%

反応手順

To a stirred solution of N-methoxy-N-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide (6.54 g, 24.8 mmol, Step-2) in THF (80 mL) is added dropwise 1.06M methylmagnesium bromide (46.7 mL, 49.5 mmol) at 0° C. The reaction mixture is stirred at rt for 1.5 hours. The reaction mixture is poured into saturated aqueous sodium hydrogen carbonate (100 mL) and extracted with EtOAc (300 mL). The organic layer is washed with water (100 mL×2) and dried over sodium sulfate. After filtration, the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with n-hexane/EtOAc (1:1) to give 4.51 g (83% yield) of the title compound as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187475B2
出典データセットuspto-grants-2015_11
ORD IDord-05fd2e2e06eb4df8aec4e35d9f662de3
出典メモuspto-grants-2015_11