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HRID 2251696作成日:2026年10月25日

4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide → 2-Methyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid

https://huagongshe.com/reaction/2251696

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5-Amino-2-methylbenzoic acidHCID 10374614—
溶媒DimethylformamideHCID 6228—
生成物2-Methyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acidHCID 1033978727%

反応手順

According to the similar procedure in Synthesis Example 1, by using 5-amino-2-methylbenzoic acid (2.06 g, 15.0 mmole), DMF (60 ml), TEA (4 ml), and 2,3,5,6-tetrafluoro-4-trifluoromethylbenzyl bromide (5.52 ml, 17.7 mmole), 1.50 g (27.0% yield) of 2-methyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid was obtained as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07319160B2
出典データセットuspto-grants-2008_01
ORD IDord-24e0744e439648d3aba7c9608dceea84
出典メモuspto-grants-2008_01