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HRID 902741作成日:2026年10月26日

2-(4-Methoxyphenyl)propan-1-amine → N-(2-Chloro-3-trifluoromethylbenzyl)-2-(4-methoxyphenyl)propylamine

https://huagongshe.com/reaction/902741

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Methoxyphenyl)propan-1-amineHCID 202625—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物2-Chloro-3-(trifluoromethyl)benzaldehydeHCID 2736672—
溶媒MethanolHCID 887—
溶媒Diethyl EtherHCID 3283—
生成物N-(2-Chloro-3-trifluoromethylbenzyl)-2-(4-methoxyphenyl)propylamineHCID 6925485477%

反応手順

A solution of 2-(4-methoxyphenyl)propylamine (183 mg, 1.11 mmole) and 2-chloro-3-trifluoromethylbenzaldehyde (230 mg, 1.11 mmole) in 10 mL of MeOH was treated with a crystal of p-toluenesulfonic acid hydrate, and stirred for 30 minutes. The reaction was diluted with Et2O, and washed with aqueous NaHCO3. The extracts were dried, and the solvent removed. A solution of the residue in 10 mL of MeOH was cooled to 0° and treated with excess NaBH4. The reaction was warmed to 23° and stirred for 30 minutes. The reaction was diluted with H2O and extracted with Et2O. The extracts were washed with H2O, dried and the solvent removed, and gave the titled compound, 305 mg (77% yield). MS (ESI) 358 (MH+)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365085B2
出典データセットuspto-grants-2008_04
ORD IDord-186c9854a9884c8eb685c624d6261659
出典メモuspto-grants-2008_04