反应 #2286284
ord-e8a99a53e78d43f6b6903dc1f494f7c6
反应方程式
反应条件
后处理
- 1温度The reaction was heated
- 2温度to reflux for 24 h
- 3浓缩concentrated under vacuum
- 4workup.ADDITIONThe resulting oil was diluted with water (200 mL)
- 5workup.ADDITIONacidified to pH=2 by addition of a 1N aqueous hydrochloric acid solution
- 6萃取The water layer was extracted with ethyl acetate (300 mL)
- 7workup.ADDITIONThe water layer was made basic to pH=10 by the addition of a 1N aqueous sodium hydroxide solution
- 8萃取was extracted with ethyl acetate (2×350 mL)
- 9洗涤The organics were washed with a saturated aqueous sodium chloride solution
- 10干燥dried with magnesium sulfate
- 11过滤filtered
- 12浓缩concentrated under vacuum
- 13其他The resulting oil was dried under high vacuum overnight
实验过程
A solution of 2-chloro-6-methyl phenol (5.0 g, 0.035 mol) in ethanol (25 mL) at room temperature was treated with dimethyl amine (3.95 mL of a 40% solution of dimethylamine in water, 0.035 mol) followed by formaldehyde (2.85 mL of a 37% solution of formaldehyde in water, 0.035 mol). The reaction was heated to reflux for 24 h. At this time, the reaction mixture was cooled to room temperature and concentrated under vacuum. The resulting oil was diluted with water (200 mL) and acidified to pH=2 by addition of a 1N aqueous hydrochloric acid solution. The water layer was extracted with ethyl acetate (300 mL). The ethyl acetate layer was discarded. The water layer was made basic to pH=10 by the addition of a 1N aqueous sodium hydroxide solution and was extracted with ethyl acetate (2×350 mL). The organics were washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum. The resulting oil was dried under high vacuum overnight to afford 2-chloro-4-dimethylaminomethyl-6-methyl-phenol (2b) (4.62 g, 66%) as an off-white solid; EI(+)-HRMS m/z calcd for C10H14ClNO (M+) 199.0764, found 199.0767. Molecular Weight=199.6822; Exact Mass=199.0764