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HRID 1060060作成日:2026年10月27日

Water → 3-(4-Chloro-3-ethylphenoxy)aniline

https://huagongshe.com/reaction/1060060

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-(4-Chloro-3-ethylphenoxy)-1-nitrobenzeneHCID 11065754—
触媒ZincHCID 23994—
溶媒Acetic AcidHCID 176—
生成物3-(4-Chloro-3-ethylphenoxy)anilineHCID 11021230112.1%

反応手順

EX-8B) To a solution of 3-(4-chloro-3-ethylphenoxy)-1-nitrobenzene (10 g, 0.036 mol) from EX-A in 400 mL of glacial acetic acid and 1 mL of water was added zinc metal (20 g, 0.305 mol) at room temperature, and the resultant mixture was stirred for 1 h. The reaction mixture was filtered through celite. The filtrate was neutralized with ammonium hydroxide and extracted with diethyl ether. The organic layer was washed with water and brine, dried over MgSO4, and concentrated in vacuo to give 10 g (100%) of the desired 3-(4-chloro-3-ethylphenoxy)aniline product as a dark orange oil, which was greater than 90% pure by reverse phase HPLC analysis. HRMS calcd. for C14H14ClNO: 248.0842 [M+H]+, found: 248.0833.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06521607B1
出典データセットuspto-grants-2003_02
ORD IDord-f20a67beeb5347b0b2a98e1eefd2e43f
出典メモuspto-grants-2003_02