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ChemicalBook CAS DataBase List 3-formylpropiononitrile
3515-93-3

3-formylpropiononitrile synthesis

11synthesis methods
-

Yield:3515-93-3 98%

Reaction Conditions:

with hydrogenchloride;water in acetone at 0; for 9 h;

Steps:

14

Example 14; 4-Oxobutanenitrile (31).; A mixture of 4,4-diethoxybutanenitrile (30, 0.95 g,6.0 mmol), acetone (30 mL), and 6 N HCl (12 mL) was stirred at 0 0C for 9 h. After the reaction was complete, the mixture was concentrated to approximately 2 mL and was extracted with chloroform (4 x- 10 mL). The combined organic phase was dried with sodium sulfate. The solvent was removed by rotary evaporation to give crude 31 EPO as an oil (0.49 g, 98%). 1H NMR (400 MHz, CDCl3) £9.8 (s, IH), 2.9 (t, 2H, J = 7.2 Hz), 2.6 (t, 2H5 J= 7.2 Hz).

References:

WO2007/35964,2007,A2 Location in patent:Page/Page column 9; 15-16

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