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HRID 551894作成日:2026年10月27日

Sodium Chloride → {4-[(4-Butylphenyl)ethynyl]benzyl}[2-(4-chlorophenyl)ethyl]amine

https://huagongshe.com/reaction/551894

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物2-(4-Chlorophenyl)ethylamineHCID 67430—
反応物Sodium borohydrideHCID 4311764—
反応物4-[2-(4-Butylphenyl)ethynyl]benzaldehydeHCID 11334512—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物{4-[(4-Butylphenyl)ethynyl]benzyl}[2-(4-chlorophenyl)ethyl]amineHCID 5755450773.6%

反応条件

温度0 °C

反応手順

A solution of 4-[(4-butylphenyl)ethynyl]benzaldehyde (2.62 g, 10.0 mmol, intermediate to which may be obtained according to methods disclosed in EP03103780.7) and 2-(4-chlorophenyl)ethylamine (Aldrich, 1.56 g, 10 mmol) was heated at reflux in toluene (50 mL) for 12 hrs with azeotropic removal of water. The mixture was evaporated under vacuum and the residue was taken up in MeOH (60 mL) and chilled at 0° C. NaBH4(567 mg, 15.0 mmol) was added portionwise and the reaction mixture was stirred for 30 min at 0° C. and 3 hrs at rt. The reaction mixture was poured into a saturated solution of NaCl and extracted with Et2O. The combined organic layers were dried over MgSO4 and the solvents were removed under reduced pressure to give the crude product. Purification by chromatography on silicagel (EtOAc/c-hex 30/70) gave 2.96 g (54%) of the title compound as a white solid. HPLC, Rt: 5.0 min (purity: 99.9%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947851B2
出典データセットuspto-grants-2011_05
ORD IDord-45b22b9d1eb24b8c960859287ac9e5ce
出典メモuspto-grants-2011_05