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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 964489생성일: 2026년 10월 25일

Methyl 3-carbamoyl-5-nitrobenzoate → Methyl 3-(aminomethyl)-5-nitrobenzoate

https://huagongshe.com/reaction/964489

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-carbamoyl-5-nitrobenzoateHCID 3741295—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-(aminomethyl)-5-nitrobenzoateHCID 1907713234.4%

반응 단계

A mixture of 3-methoxycabonyl-5-nitrobenzamide (1120 mg, 5 mmol) and 1M BH3 in THF (11.5 mL) was refluxed for 90 minutes. The solvent was evaporated and MeOH (15 mL) was added. HCl gas was introduced into the solution and the reaction mixture was refluxed for 70 minutes. The mixture was added saturated NaHCO3 aq. (50 mL) and extracted with CH2Cl2 (5×40 mL). The organic layers were combined, washed with brine and dried over Na2SO4. The dried solution was applied directly to SiO2 column and developed with AcOEt then 1/10=MeOH/AcOEt. The elution was evaporated to give the desired product (361 mg, 34%): 1H NMR (300 MHz, CDCl3) δ 8.696 (s, 1H), 8.403 (s, 1H), 8.320 (s, 1H), 4.051 (s, 2H), 3.961 (s, 3H); 13C NMR (300 MHz, CDCl3) δ 165.0, 148.3, 145.9, 133.7, 131.7, 125.8, 122.8, 52.7, 45.2; HRMS m/e calc'd for C9H10N2O4 : 209.0562, found 209.0565.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05770380
출처 데이터셋uspto-grants-1998_06
ORD IDord-0beba088adde475faed41b2ee72c086b
출처 메모uspto-grants-1998_06