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HRID 964489作成日:2026年10月25日

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

https://huagongshe.com/reaction/964489

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-carbamoyl-5-nitrobenzoateHCID 3741295—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-(aminomethyl)-5-nitrobenzoateHCID 1907713234.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05770380
出典データセットuspto-grants-1998_06
ORD IDord-0beba088adde475faed41b2ee72c086b
出典メモuspto-grants-1998_06