反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 60 °C
PROCEDURE
实验过程
A solution of 2-(5-fluoro-2-methoxyphenyl)-2-hydroxy-N,N-dimethylethanethioamide (0.5 g, 2.1 mmol) in Eaton's reagent (5 mL) were combined and heated rapidly to 60° C. and left for 1 h. After cooling to room temperature over 2 hours the mixture was dropwise addition into prechilled aqueous sodium hydroxide (2 N, 16.25 mL) with constant stirring. This solution was then extracted with methyl tert-butyl ether (5×20 mL) and the combined organic extracts were dried (MgSO4) and the solvent removed in vacuo to give a yellow solid. This was purified by flash chromatography with a gradient of 0–2% diethyl ether in hexane and gave 0.2 g of yellow solid containing an impurity, this was triturated with hexane to leave a colourless solid (0.155 g, 34%) of the title compound; δH (300 MHz, CDCl3) 6.70–6.52 (2H, m, ArH), 6.12–6.10 (1H, m, ArH) 3.90 (3H, s, OCH3) and 3.2 (6H, s, N(CH3)2), M+H=226.1.
WORKUP
后处理
- temperatureAfter cooling to room temperature over 2 hours the mixture
- extractionThis solution was then extracted with methyl tert-butyl ether (5×20 mL)
- dry with materialthe combined organic extracts were dried (MgSO4)
- customthe solvent removed in vacuo
- customto give a yellow solid
- customThis was purified by flash chromatography with a gradient of 0–2% diethyl ether in hexane