戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 913896作成日:2026年10月26日

N-Iodosuccinimide → 3-Bromo-2-iodo-5-(trifluoromethyl)aniline

https://huagongshe.com/reaction/913896

反応式

関与物質

役割名称HCID仕込み量
反応物N-IodosuccinimideHCID 120273—
反応物3-Bromo-5-(trifluoromethyl)anilineHCID 2735880—
溶媒Acetic AcidHCID 176—
溶媒Ethyl AcetateHCID 8857—
生成物3-Bromo-2-iodo-5-(trifluoromethyl)anilineHCID 57546142—

反応手順

3-Bromo-5-(trifluoromethyl)aniline (20 g, 83 mmol) in acetic acid (150 ml) was treated portionwise with N-iodosuccinimide (20.62 g, 92 mmol). The reaction was stirred 24 h at ambient temperature. The reaction was diluted with ethyl acetate (600 mL) and was washed with aqueous sodium bisulfie (100 mL) and brine (100 mL). The organic layer was dried with magnesium sulfate and evaporated. The residue was purified on a silica gel column with a gradient of ethyl acetate/hexanes from 7% to 15% to give 23.5 g (77%) of slightly impure product. 1H-NMR (CDCl3, 400 MHz) δ 7.21 (d, J=1.3 Hz, 1H), 6.82 (d, J=1.5 Hz, 1H), 4.57 (bs, 2H); LC/MS (HPLC method 4): tR=3.578 min, 365.80(MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08026257B2
出典データセットuspto-grants-2011_09
ORD IDord-24bf3eb8f2554ac5ae473672e1b1b61d
出典メモuspto-grants-2011_09