戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1964331作成日:2026年10月24日

Trifluoroacetic acid → (2-(Tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amine

https://huagongshe.com/ja/reaction/1964331

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物2-Iodo-4-nitroanilineHCID 222629—
反応物2-((Tert-butyldimethylsilyl)oxy)acetaldehydeHCID 4187788—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒MethanolHCID 887—
生成物(2-(Tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amineHCID 5912939325%

反応手順

To a solution of 2-iodo-4-nitroaniline (2.0 g, 7.6 mmol) and 2-(tert-butyldimethylsilyloxy)-acetaldehyde (3.5 g, 75% purity, 15 mmol) in methanol (30 mL) was added TFA (1.5 mL) at 0° C. The reaction mixture was stirred at this temperature for 30 min before NaCNBH3 (900 mg, 15 mmol) was added in portions. The mixture was stirred for 2 h and was then quenched with water. The resulting mixture was extracted with EtOAc (30 mL×3), the combined organic extracts were dried over anhydrous Na2SO4 and evaporated under vacuum, and the residue was purified by chromatography on silica gel (5% ethyl acetate/petroleum) to afford [2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-(2-iodo-4-nitro-phenyl)-amine (800 mg, 25%). 1H NMR (300 MHz, CDCl3) δ 8.57 (d, J=2.7 Hz, 1 H), 8.12 (dd, J=2.4, 9.0 Hz, 1 H), 6.49 (d, J=9.3 Hz, 1 H), 5.46 (br s, 1 H), 3.89 (t, J=5.4 Hz, 2 H), 3.35 (q, J=5.4 Hz, 2 H), 0.93 (s, 9 H), 0.10 (s, 6 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415387B2
出典データセットuspto-grants-2013_04
ORD IDord-0fdb3c61171a4891b777ee6e94b078b4
出典メモuspto-grants-2013_04