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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1767017생성일: 2026년 10월 26일

Morpholine → 2-Methyl-4-morpholino-6-nitroaniline

https://huagongshe.com/reaction/1767017

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물4-Bromo-2-methyl-6-nitroanilineHCID 522679—
반응물2-(Di-tert-butylphosphino)biphenylHCID 2734215—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TetrahydrofuranHCID 8028—
생성물2-Methyl-4-morpholino-6-nitroanilineHCID 11601132—

반응 조건

온도85 °C

반응 단계

To a 800 ml pressure flask was added Tris(dibenzylideneacetone)dipalladium (2.64 g, 2.88 mmol), 2-(Di-t-butylphosphino)biphenyl (1.42 g, 4.75 mmol) and sodium tert-butoxide (17.5 g, 182 mmol). Then dry THF (500 mL), 4-bromo-2-methyl-6-nitroaniline (30.0 g, 130 mmol) and morpholine (34 ml, 390 mmol) were added. Argon was bubbled through the solution for 1 minute and the flask was sealed. The reaction mixture was stirred at 85° C. for 3 days. THF was evaporated in vacuo and the crude product was preabsorbed on silica and this then transferred on top of a silica gel column. Elution with hexane-ethyl acetate (6:4 to 4:6 to 0:1 gradient) gave, after evaporation of solvents, the title compound (15.2 g red-brown solid, 49.3%). LCMS (M+H)+ m/z 238 (t=0.64 min.) 1H NMR (500 MHz, DMSO-d6) δ 7.32 (1H, s), 7.22 (1H, s), 6.96 (2H, s), 3.72 (4H, broad s), 2.96 (4H, broad s), 2.21 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07232826B2
출처 데이터셋uspto-grants-2007_06
ORD IDord-ae5192d442f747f2bf399f3868f69d6f
출처 메모uspto-grants-2007_06