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HRID 1985939作成日:2026年10月25日

Ethanol → 3,3,3-Trifluoro-2-(trifluoromethyl)-1-(hydroxymethyl)propylamine

https://huagongshe.com/reaction/1985939

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Ethyl AcetateHCID 8857—
反応物4,4,4,4',4',4'-HexafluorovalineHCID 85954—
反応物Borane;tetrahydrofuranHCID 2723981—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3,3,3-Trifluoro-2-(trifluoromethyl)-1-(hydroxymethyl)propylamineHCID 45107971—

反応条件

温度25 °C

反応手順

A solution of 4,4,4,4′,4′,4′-hexafluoro-DL-valine (0.500 g, 2.22 mmol) in THF (20 mL) was stirred under nitrogen at 25° C. Borane-THF complex (6.66 mL, 1.0 M in THF) was added dropwise and the resulting solution stirred for 4 h at 25° C. After this time period, the reaction was complete by TLC (10:2:1 EtOAc:EtOH:H2O). The reaction mixture was quenched by slow addition of 10% HOAc in MeOH (23 mL). After concentration, the residue was dissolved in Et2O (200 mL) and washed with saturated aqueous NaHCO3 (3×20 mL) and brine (20 mL), and then dried using Na2SO4. After concentration, the resulting residue was used directly in the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07547725B2
出典データセットuspto-grants-2009_06
ORD IDord-572a1b43fd71487f8387137449386527
出典メモuspto-grants-2009_06