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HRID 1667170作成日:2026年10月27日

Ethyl bromoacetate → Ethyl 2-(3,3-bis(4-fluorophenyl)-2-oxopiperidin-1-yl)acetate

https://huagongshe.com/reaction/1667170

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物Potassium tert-butoxideHCID 23665647—
反応物3,3-Bis(4-fluorophenyl)piperidin-2-oneHCID 67357646—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-(3,3-bis(4-fluorophenyl)-2-oxopiperidin-1-yl)acetateHCID 67359841—

反応条件

温度80 °C

反応手順

To the product from Example 90B (0.43 g, 1.50 mmol) as a solution in tetrahydrofuran (20 mL) was added potassium tert-butoxide (1.0 M in tetrahydrofuran) (1.80 mL, 1.80 mmol) via syringe under nitrogen followed by the addition of ethyl 2-bromoacetate (0.18 mL, 1.65 mmol). The reaction mixture heated at 80° C. and stirred overnight. The reaction mixture was cooled to room temperature, concentrated, diluted with ethyl acetate, washed with water and brine, dried with MgSO4, filtered and concentrated. Silica gel chromatography eluting with ethyl acetate/hexane (1:4) gave the title compound. MS (DCI) m/z 374 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044069B2
出典データセットuspto-grants-2011_10
ORD IDord-4495887aaf8546ff838da280f2868dde
出典メモuspto-grants-2011_10