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HRID 733304作成日:2026年10月26日

3,5-Di-tert-butylphenol → 2-(1-Aminoethyl)-3,5-di-tert-butylphenol

https://huagongshe.com/reaction/733304

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Di-tert-butylphenolHCID 70825—
反応物N-(1-Isopropoxyethyl)acetamideHCID 14204909—
溶媒Trifluoroacetic acidHCID 6422—
生成物2-(1-Aminoethyl)-3,5-di-tert-butylphenolHCID 10467261—

反応手順

To a solution of 2.06 g (10.0 mmol) of 3,5-di-tert-butylphenol in 10 mL of trifluoroacetic acid was added 1.6 g (11.0 mmol) of N-(1-isopropoxyethyl)acetamide and the resulting mixture was stirred overnight at room temperature. The reaction mixture was concentrated in vacuo, and the residue was partitioned between EtOAc and saturated aqueous NaHCO3. The aqueous layers were separated and then extracted with EtOAc. The organic layers were combined, dried (Na2SO4), filtered and evaporated in vacuo. The product was purified on a silica gel flash chromatogrohy column eluted with 0-25% EtOAc in CH2Cl2. Evaporation of the purified fraction and drying in vacuo afforded the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589127B2
出典データセットuspto-grants-2009_09
ORD IDord-2cecf6c87c3944a8b21ff657b0f7978d
出典メモuspto-grants-2009_09