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HRID 322561作成日:2026年10月26日

Ethanol → (R)-3-(3-Fluorophenoxy)-3-phenylpropylamine

https://huagongshe.com/reaction/322561

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Ammonium HydroxideHCID 14923—
反応物Maleic AcidHCID 444266—
反応物(R)-3-(3-Fluorophenoxy)-3-phenylpropylchlorideHCID 39364375—
溶媒Ethyl AcetateHCID 8857—
生成物(R)-3-(3-Fluorophenoxy)-3-phenylpropylamineHCID 11593957—

反応手順

A solution of (R)-3-(3-fluorophenoxy)-3-phenylpropyl chloride (0.971 g, 3.96 mmol), conc. NH4OH (30 mL), and EtOH (20 mL) were shaken at 90° C. on a Parr' apparatus (50-90 psig) for 18 h. The mixture was then evaporated under vacuum and the residue was dissolved in Et2O (100 mL) and washed with H2O (2×25 mL). The organic layer was dried (anh. Na2SO4), filtered, and evaporated under vacuum to provide a yellow oil. This material was then dissolved in EtOAc (50 mL) and filtered. A solution of maleic acid (0.272 g, 2.6 mmol, 0.93 equiv) dissolved in hot EtOAc (5 mL) was added to precipitate the maleate salt (519 mg, 53.5%) as a white solid: TLC Rf 0.25 (1% MeOH-CHCl3); GC, tr 7.37 min; MS, m/z 245 (M+). The synthesis of Compound 187 was accomplished as follows.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211245B1
出典データセットuspto-grants-2001_04
ORD IDord-b6c9877bcb704dbf907dab274b2c6d8b
出典メモuspto-grants-2001_04