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HRID 8461作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/8461

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium borohydrideHCID 4311764—
反応物Methyl (2S)-2-(2,3,4-trifluoroanilino)propionateHCID 10125210—
溶媒WaterHCID 962—
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 IPE (0.2 ml). Then a solution (0.8 ml) of methyl (2S)-2-(2,3,4-trifluoroanilino)propionate (200 mg, 99.8% ee) in IPE was added to the solution. After adding methanol (137.4 mg), the liquid reaction mixture was stirred for 2 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 176 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-114c8b0cd3ee46b0b31d316ba3f13637
出典メモuspto-grants-2006_08