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HRID 470408作成日:2026年10月25日

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

https://huagongshe.com/reaction/470408

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US08629138B2
出典データセットuspto-grants-2014_01
ORD IDord-87e1f83152c54fa0bba0099047097100
出典メモuspto-grants-2014_01