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
To a 500 ml eggplant-shaped flask were added 25.00 g (78.32 mmol) 2-bromo-1-(4-methoxy-phenyl)-3-phenyl-propan-1-one prepared in the step 3 and 150 ml anhydrous ethanol, then added 5.96 g (78.32 mmol) thiourea and 6.42 g (78.32 mmol) anhydrous sodium acetate under stirring, the resulting mixture was stirred at room temperature for 1 hour, then refluxed for 2 hours, and cooled to room temperature, and a solid was precipitated, filtered, washed with water, dried to obtain 18.01 g of a product, a single spot was shown by TLC, the product was not further purified in a yield of 77.6%, mp: 177-178□. 1H-NMR (DMSO-d6, 400 MHz) δ: 3.76 (3H, s, OCH3), 4.04 (2H, s, CH2), 6.82 (2H, s, NH2), 6.93 (2H, d, J=9.00 Hz, ArH), 7.18˜7.35 (5H, m, ArH), 7.46 (2H, d, J=9.00 Hz, ArH); EI-MS m/e (%): 296.1 (M, 100), 219.0 (19); HREI-MS Calcd. for C17H16N2OS: 296.0983. found: 296.0978. Anal. Calcd. for C17H16N2OS: C, 68.89; H, 5.44; N, 9.45. found: C, 69.08; H, 5.32; N, 9.57.
WORKUP
后处理
- stirringthe resulting mixture was stirred at room temperature for 1 hour
- temperaturerefluxed for 2 hours
- customa solid was precipitated
- filtrationfiltered
- washwashed with water
- customdried