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HRID 1791854作成日:2026年10月26日

t-Butoxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene → Amino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene

https://huagongshe.com/reaction/1791854

反応式

関与物質

役割名称HCID仕込み量
反応物t-Butoxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 22033517—
溶媒Hydrochloric AcidHCID 313—
溶媒Ethyl AcetateHCID 8857—
生成物Amino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 2203354021.8%

反応手順

t-Butoxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene (2.69 g, 7.64 mmol; from step (ii) above) were dissolved in EtOAc, pre-saturated with HCl(g), (150 mL) under nitrogen and stirred at room temperature overnight. After evaporation of the solvent the residue was partitioned between 10% aqueous HCl and EtOAc. The aqueous phase was washed with EtOAc, basified with NaOH (2M, aq.) and extracted with EtOAc. The combined organic phases were washed with brine, dried (MgSO4) and the solvent evaporated to afford 0.42 g (19%) of the sub-title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07074820B2
出典データセットuspto-grants-2006_07
ORD IDord-5072aaaf7af947d3ab046709fd2cf87e
出典メモuspto-grants-2006_07