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HRID 584023作成日:2026年10月26日

4-(2,6-Dimethyl-4-nitrophenoxy)-2-(4-fluorobenzenesulfonyl)phenol → 4-(4-Amino-2,6-dimethylphenoxy)-2-(4-fluorobenzenesulfonyl)phenol

https://huagongshe.com/reaction/584023

反応式

関与物質

役割名称HCID仕込み量
反応物4-(2,6-Dimethyl-4-nitrophenoxy)-2-(4-fluorobenzenesulfonyl)phenolHCID 22344899—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒Ethyl AcetateHCID 8857—
生成物4-(4-Amino-2,6-dimethylphenoxy)-2-(4-fluorobenzenesulfonyl)phenolHCID 2234487698.9%

反応手順

To a solution of 4-(2,6-dimethyl-4-nitro-phenoxy)-2-(4-fluoro-benzenesulfonyl)-phenol (11.4 g, 27.4 mmol) in a mixture of ethanol (200 mL) and EtOAc (200 mL) was added catalyst (10% Pd/C, 2.29 g). The mixture was hydrogenated under 45 psi at RT for 4 h. The mixture was filtered through Celite and concentrated to give the title compound of Step D (10.5 g) as a tan solid. The title product of Step D was used in the next step with no further purification. MS (APCl−) Calc.:387.1. Found: 386.2 (M−1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06924310B2
出典データセットuspto-grants-2005_08
ORD IDord-73effbb231db4d2f8ebf83ecdf676444
出典メモuspto-grants-2005_08