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HRID 705820作成日:2026年10月27日

Ammonium Chloride → 3-(2,4,6-Trifluoro-phenyl)-acrylic acid ethyl ester

https://huagongshe.com/reaction/705820

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Ethyl (dimethoxyphosphinoyl)acetateHCID 67555—
反応物2,4,6-TrifluorobenzaldehydeHCID 521845—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
溶媒tetrahydrofuran N,N-dimethylformamideHCID 21974620—
生成物3-(2,4,6-Trifluoro-phenyl)-acrylic acid ethyl esterHCID 5741277987%

反応手順

To the solution of ethyl[bis(methyloxy)phosphoryl]acetate (1.980 mL, 11.99 mmol) in THF-DMF (60 mL, v/v=5:1) at 0° C. was added t-BuOK (1.458 g, 12.99 mmol) portion wise. The resultant mixture was stirred at room temperature for 30 minutes, then mixed with a solution of 2,4,6-trifluorobenzaldehyde (1.6 g, 9.99 mmol) in THF (10 mL) at 0° C. It was allowed to warm to room temperature and the mixture was stirred for 45 min. It was mixed with aqueous ammonium chloride and then extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified by a flash column chromatography to give the title compound as a pale yellow oil (2.0 g, 87% yield). LCMS: rt=3.52 min, [M+H+]=231.1

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09174968B2
出典データセットuspto-grants-2015_11
ORD IDord-bd4f57bd21b948e78237edfbdb833036
出典メモuspto-grants-2015_11