反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A turbid, yellow-orange solution of sodium nitromalonaldehyde monohydrate (15.7 mg, 0.10 mmol) in DMF (275 uL) and water (25 uL) was added dropwise over a 2 min period to a solution of benzylamine (27.4 uL, 0.25 mmol) in DMF (165 uL), water (15 uL) and 96% formic acid (0.94 uL, 0.025 mmol) and was stirred at room-temperature for 24 h. A few drops of the reaction mixture were added to ˜1 mL water giving a white, opaque emulsion that was extracted with EtOAc twice. The combined organics were dried over Na2SO4, evaporated under N2 and dried in vacuo at room-temperature to give 3.0 mg of the crude title compound (I1) as a pale-pink residue (3.0 mg, 10% crude yield); HRMS calcd for C17H18N3O2 (M+H+) 296.13990, obsd 296.13733 (100%); 1H NMR (300 MHz, DMSO-d6) δ 4.719 (s, 4H), 7.274-7.304 (m, 10H), 8.898 (s, 2H), ˜11.7 (br s, 1H).
WORKUP
后处理
- extractionwas extracted with EtOAc twice
- dry with materialThe combined organics were dried over Na2SO4
- customevaporated under N2
- customdried in vacuo at room-temperature