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HRID 1187795作成日:2026年10月27日

Acetic Acid → 4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-ol

https://huagongshe.com/reaction/1187795

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物(alphaS)-4-Bromo-alpha-methylbenzenemethanamineHCID 852999—
反応物3-Hydroxy-4-methoxy-3-phenyl-butyraldehydeHCID 59635677—
溶媒TetrahydrofuranHCID 8028—
生成物4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-olHCID 59635799—

反応手順

(S)-1-(4-Bromo-phenyl)-ethylamine (0.93 g), NaB(OAc)3 (0.98 g), and acetic acid (0.27 mL) were added in the given order to a solution of 3-hydroxy-4-methoxy-3-phenyl-butyraldehyde (0.90 g) in tetrahydrofuran (20 mL) at ca. 10-15° C. The cooling bath was removed and the mixture was stirred at room temperature for 2 h. Then, water (50 mL) and 1 M aqueous NaOH solution (20 mL) were added and the resulting mixture was stirred for another 30 min. The mixture was extracted with ethyl acetate and the combined extracts were washed with water and brine. After drying (MgSO4), the solvent was removed to give the title compound which was submitted to the subsequent reaction step without further purification. Yield: 1.80 g (quantitative).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08673899B2
出典データセットuspto-grants-2014_03
ORD IDord-cb55549e13d645ecb216ea5e0f73b3ab
出典メモuspto-grants-2014_03