反应 #792141

反应方程式

sodium cyanoborohydride

acetic acid

1-(indan-2-yl)ethanone

cyclopropylamine

→

N-[1-(indan-2-yl)ethyl]cyclopropanamine

收率 28.0%

溶剂

methanol

反应条件

后处理

1. 1
   温度at reflux
2. 2
   workup.STIRRINGthe reaction mixture is further stirred for 2 hrs
3. 3
   温度at reflux
4. 4
   其他The cooled reaction mixture
5. 5
   过滤is then filtered over a cake of diatomaceous earth
6. 6
   洗涤The cake is washed twice by 80 ml of methanol
7. 7
   浓缩the combined methanolic extracts are concentrated under vacuum
8. 8
   workup.ADDITION100 ml of water are then added to the residue
9. 9
   萃取The watery layer is extracted with 300 ml of ethyl acetate
10. 10
    洗涤The organic layer is washed twice by brine
11. 11
    过滤filtered over a phase separator paper
12. 12
    其他to yield after concentration 5 g of a yellow oil

实验过程

To a cooled solution of 3.5 g (21.8 mmol) of 1-(indan-2-yl)ethanone in 100 ml of methanol, are added 10 g of 3 Å molecular sieves and 2.3 g (40.2 mmol) of cyclopropylamine followed by a slow addition of 2.87 ml (50.2 mmol) of acetic acid. The reaction mixture is stirred for 2.5 hrs at reflux. The reaction mixture is then cooled to 0° C. and 1.9 g (30 mmol) of sodium cyanoborohydride are slowly added and the reaction mixture is further stirred for 2 hrs at reflux. The cooled reaction mixture is then filtered over a cake of diatomaceous earth. The cake is washed twice by 80 ml of methanol and the combined methanolic extracts are concentrated under vacuum. 100 ml of water are then added to the residue and the pH is ajusted to 12 with a 0.5 N solution of sodium hydroxyde. The watery layer is extracted with 300 ml of ethyl acetate. The organic layer is washed twice by brine and filtered over a phase separator paper to yield after concentration 5 g of a yellow oil. Column chromatography on silica gel (gradient heptane/ethyl acetate) yields 1.2 g (28% yield) of N-[1-(indan-2-yl)ethyl]cyclopropanamine as a colourless oil (M+H =202).

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