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HRID 520359作成日:2026年10月24日

tert-Butylsulfinamide, (S)-(-)- → (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate

https://huagongshe.com/ja/reaction/520359

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butylsulfinamide, (S)-(-)-HCID 11355477—
反応物Ethyl 4-fluoro-3,3-dimethyl-2-oxobutanoateHCID 86690078—
触媒HCID 178477244HCID 178477244—
溶媒Sodium ChlorideHCID 5234—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoateHCID 8669007930.2%

反応条件

温度65 °C

反応手順

To a solution of ethyl 4-fluoro-3,3-dimethyl-2-oxobutanoate (2.3 g, 13.05 mmol) in THF (20 mL) was added (S)-2-methylpropane-2-sulfinamide (1.899 g, 15.67 mmol) and tetraethoxytitanium (5.91 mL, 26.1 mmol). The reaction mixture was heated at 65° C. for 6 h. The reaction mixture was cooled down, diluted with EtOAc and sat. NaCl (40 mL) and stirred at rt for 0.5 h. The solid was filtered and washed with water and EtOAc. The filtrate was separated and the organic layer was washed with water, sat. NaCl, dried (MgSO4) and purified by flash chromatography (EtOAc/hexane) to afford (S)-ethyl 2-(tert-butylsulfinylimino)-4-fluoro-3,3-dimethylbutanoate (1.1 g). 1H NMR (400 MHz, CDCl3) δ ppm 4.46-4.53 (1H, m), 4.28-4.42 (3H, m), 1.59 (3H, s), 1.21-1.31 (15H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09326973B2
出典データセットuspto-grants-2016_05
ORD IDord-123710cb3b9642a2a1939182945b1418
出典メモuspto-grants-2016_05