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HRID 584865作成日:2026年10月26日

4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide → 2-Nitro-4-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)phenol

https://huagongshe.com/reaction/584865

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
反応物4-Amino-2-NitrophenolHCID 3417419—
溶媒DimethylformamideHCID 6228—
生成物2-Nitro-4-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)phenolHCID 1043007540.1%

反応手順

According to the similar procedure in Synthesis Example 1, by using 4-amino-2-nitrophenol (1.00 g, 6.49 mmole), DMF (30 ml), TEA (0.5 ml), and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (1.30 g, 7.78 mmole), 1.00 g (40.0% yield) of 2-nitro-4-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)phenol was obtained as a reddish solid.:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06927303B2
出典データセットuspto-grants-2005_08
ORD IDord-56c55971ff944e42afbb4057312797f6
出典メモuspto-grants-2005_08