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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468358생성일: 2026년 10월 25일

Benzenamine, 2-bromo-4-nitro- → 2-((1-Methylcyclopropyl)ethynyl)-4-nitroaniline

https://huagongshe.com/reaction/468358

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참여 물질

역할이름HCID투입량
반응물Benzenamine, 2-bromo-4-nitro-HCID 25840—
반응물1-Ethynyl-1-methylcyclopropaneHCID 21590560—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TriethylamineHCID 8471—
생성물2-((1-Methylcyclopropyl)ethynyl)-4-nitroanilineHCID 5912951979%

반응 조건

온도70 °C

반응 단계

To a deoxygenated solution of 2-bromo-4-nitroaniline (430 mg, 2.0 mmol) and 1-ethynyl-1-methyl-cyclopropane (630 mg, 8.0 mmol) in triethylamine (20 mL) was added CuI (76 mg, 0.40 mmol) and Pd(PPh3)2Cl2 (140 mg, 0.20 mmol) under N2. The mixture was heated at 70° C. and stirred for 24 h. 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-((1-methylcyclopropyl)ethynyl)-4-nitroaniline (340 mg, 79%). NMR (300 MHz, CDCl3) δ 8.15-8.14 (m, 1H), 7.98-7.95 (m, 1H), 6.63 (d, J=6.9 Hz, 1H), 4.80 (brs, 2H), 1.38 (s, 3H), 1.04-1.01 (m, 2H), 0.76-0.73 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623905B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-9df49c113925456391c56a16c62783ca
출처 메모uspto-grants-2014_01