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HRID 8458作成日:2026年10月23日

Methanol → (2S)-2-(2,3,4-Trifluoroanilino)propanol

https://huagongshe.com/ja/reaction/8458

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物WaterHCID 962—
反応物Sodium borohydrideHCID 4311764—
反応物Methyl (2S)-2-(2,3,4-trifluoroanilino)propionateHCID 10125210—
溶媒ChlorobenzeneHCID 7964—
生成物(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—

反応手順

At room temperature, sodium borohydride (35.7 mg) was suspended in chlorobenzene (0.2 ml). Then a solution (0.8 ml) of methyl (2S)-2-(2,3,4-trifluoroanilino)propionate (200 mg, 99.8% ee) in chlorobenzene was added to the solution. After adding methanol (137.4 mg), the liquid reaction mixture was stirred for 6 hours. Then water was added to the liquid reaction mixture followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of ammonium chloride and dried over anhydrous magnesium sulfate. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography to thereby give 162.9 mg (99.8% ee) of the title compound as an oily substance. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 51.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087778B2
出典データセットuspto-grants-2006_08
ORD IDord-4b3497d821714899838080df19bf8f51
出典メモuspto-grants-2006_08