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HRID 855300作成日:2026年10月25日

Phenethylamine, m-trifluoromethyl- → [4-(1,1-Dimethylpropyl)-benzyl]-[2-(3-trifluoromethylphenyl)-ethyl]-amine

https://huagongshe.com/reaction/855300

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethylamine, m-trifluoromethyl-HCID 104223—
反応物4-(2-Methylbutan-2-yl)benzaldehydeHCID 473780—
反応物Sodium borohydrideHCID 4311764—
反応物(4-Cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amineHCID 69342889—
生成物[4-(1,1-Dimethylpropyl)-benzyl]-[2-(3-trifluoromethylphenyl)-ethyl]-amineHCID 6934194594%

反応手順

The title compound was synthesized in analogy to (4-cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amine (described in example S53) using 4-(1,1-dimethylpropyl)-benzaldehyde (prepared as described in example S103) (88 mg, 0.50 mmol), 2-(3-trifluoromethylphenyl)-ethylamine (94 mg, 0.50 mmol) and sodium borohydride (28 mg, 0.75 mmol). The desired product (163 mg, 94%) was isolated without further purification as a colorless oil. MS (ISP) 350.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07259183B2
出典データセットuspto-grants-2007_08
ORD IDord-8531210324f84aca98814047268ec9b2
出典メモuspto-grants-2007_08