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HRID 930413作成日:2026年10月24日

Ethyl Acetate → (NE,R)-N-[1-(3-chloro-2-fluorophenyl)ethylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/ja/reaction/930413

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium BicarbonateHCID 516892—
反応物tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
反応物1-(3-Chloro-2-fluorophenyl)ethan-1-oneHCID 11116531—
触媒HCID 178477244HCID 178477244—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物(NE,R)-N-[1-(3-chloro-2-fluorophenyl)ethylidene]-2-methylpropane-2-sulfinamideHCID 8909502996%

反応条件

温度70 °C

反応手順

To a solution of 1-(3-chloro-2-fluorophenyl)ethanone (5.60 g, 31.5 mmol) and (R)-2-methylpropane-2-sulfinamide (5.72 g, 47.2 mmol) in THF (50.0 mL) was added tetraethoxytitanium (16.50 mL, 79 mmol) and the overall bright yellow solution was heated at 70° C. for overnight. The reaction was slightly cooled with ice-water bath, then was added EtOAc (50 mL), NaHCO3 (10 mL), and brine (10 mL). The slurry was filtered through a short path of Celite and the wet cake was washed with EtOAc. The resulted bright yellow solution was phase separated, and the organic layer was concentrated to afford the title compound (8.3 g, 30.1 mmol, 96% yield) as a light yellow oil. This material was used in the next step without purification. MS m/z=276.0 [M+H]+. Calculated for C12H15ClFNOS: 275.77.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09296734B2
出典データセットuspto-grants-2016_03
ORD IDord-d619eefffc7e41c49d079b63da1b4f74
出典メモuspto-grants-2016_03