戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 19781作成日:2026年10月23日

4-tert-Butylbenzaldehyde → (4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amine

https://huagongshe.com/ja/reaction/19781

反応式

関与物質

役割名称HCID仕込み量
反応物4-tert-ButylbenzaldehydeHCID 70324—
反応物3,4-DichlorophenethylamineHCID 217958—
反応物Sodium borohydrideHCID 4311764—
触媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
生成物(4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amineHCID 68563688102.1%

反応手順

0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.227 ml 2-(3,4-dichloro-phenyl)-ethylamine (1.5 mmol) were dissolved in 4.5 ml methanol at RT, and after stirring for 30 min at RT, were refluxed for 2 h. After cooling down to RT, 85 mg (2.25 mmol) sodium borohydride were added and after stirring for 5 min at RT, the reaction mixture was then refluxed for 2 h. After cooling down to RT, the reaction mixture was treated with 4 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:2) to give 515 mg colorless viscous oil (97%). MS (ISP) 336.2 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745477B2
出典データセットuspto-grants-2010_06
ORD IDord-a189fa60b3d0427fa29e1260ede59189
出典メモuspto-grants-2010_06