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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1847398생성일: 2026년 10월 26일

Benzenamine, 2-bromo-4-nitro- → 2-(Cyclopropylethynyl)-4-nitroaniline

https://huagongshe.com/reaction/1847398

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참여 물질

역할이름HCID투입량
반응물Benzenamine, 2-bromo-4-nitro-HCID 25840—
반응물CyclopropylacetyleneHCID 138823—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TriethylamineHCID 8471—
생성물2-(Cyclopropylethynyl)-4-nitroanilineHCID 5912926223,243.199%

반응 조건

온도70 °C

반응 단계

To a deoxygenated solution of 2-bromo-4-nitroaniline (2.17 g, 0.01 mmol), ethynylcyclopropane (1 g, 15 mmol) and CuI (10 mg, 0.05 mmol) in triethylamine (20 mL) was added Pd(PPh3)2Cl2 (210 mg, 0.3 mmol) under N2. The mixture was heated at 70° C. and stirred for 24 hours. The solid was filtered off and washed with EtOAc (50 mL×3). The filtrate was evaporated under reduced pressure, and the residue was purified by column chromatography on silica gel (petroleum ether/ethyl acetate=10/1) to give 2-(cyclopropylethynyl)-4-nitroaniline (470 mg, 23%). 1H NMR (300 MHz, CDCl3) δ 8.14 (d, J=2.7 Hz, 1H), 7.97 (dd, J=2.7, 9.0 Hz, 1H), 6.63 (d, J=9.0 Hz, 1H), 4.81 (brs, 2H), 1.55-1.46 (m, 1H), 0.98-0.90 (m, 2H), 0.89-0.84 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08952050B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-f447044cdfad4da5938f209789e3f71d
출처 메모uspto-grants-2015_02