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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2060350생성일: 2026년 10월 27일

Nitrogen → 2-(Thiophen-2-yl)aniline

https://huagongshe.com/reaction/2060350

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물2-BromothiopheneHCID 13851—
반응물Sodium BicarbonateHCID 516892—
반응물2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734652—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-(Thiophen-2-yl)anilineHCID 411609792%

반응 단계

AB427 (The following reaction is carried out in an N2 atmosphere.) Dissolve Tetrakis-(triphenylphosphine)-palladium(0) (297 mg, 0.26 mmol) and 2-Bromo-thiophene (837 mg, 5.13 mmol) in DME (42 mL), degas the reaction mixture carefully (5 times) and flush with N2. After 10 min stirring add 2-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylamine (1.24 g, 5.64 mmol) and a 1M aqueous NaHCO3 solution (15.4 mL, 15.4 mmol), degas the reaction mixture again carefully (5 times) and flush with N2. Stir the mixture for 3 h at 95° C. Cool mixture to rt, remove solvent under reduced pressure and partition the residue between EtOAc and water. Extract the separated aqueous layer with EtOAc (3 times). Wash combined organic layer with brine and dry it with Na2SO4. Purify the crude product by flash chromatography (silica gel 60, CyH/EtOAc 15+1] to obtain 2-Thiophene-2-yl-phenylamine (55) as a brown solid (825 mg, 92%). 1H NMR (400 MHz, CDCl3): 4.40-6.00 (m, 2H); 6.88 (td, 1H, J1=7.6 Hz, J2=1.0 Hz); 6.93 (dd, 1H, J1=8.0 Hz, J2=1.0 Hz); 7.07 (dd, 1H, J1=5.3 Hz, J2=3.5 Hz); 7.17 (td, 1H, J1=8.0 Hz, J2=1.5 Hz) 7.22 (dd, 1H, J1=3.5 Hz, J2=1.3 Hz); 7.30 (dd, 1H, J1=7.6 Hz, J2=1.5 Hz); 7.33 (dd, 1H, J1=5.3 Hz, J2=1.3 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08278356B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-f3be26f8bf7745048b3502a9a75cf83b
출처 메모uspto-grants-2012_10