Ethyl cyanoacetate → 2-Butenoic acid, 2-cyano-3-hydroxy-, ethyl ester

Potassium carbonate (73.3 g) was added to the well stirred solution of Ethylcyanoacetate (50 g) in Dimethylformamide (250 ml) and stirred for 15 minute at ambient temperature. Acetic anhydride (90.25 g) was added drop wise to the above well stirred solution during 2 to 3 hours at ambient temperature. Reaction mixture was stirred at ambient temperature for 15 to 20 hours. Reaction mixture was diluted with water (500 ml) and extracted with dichloromethane (3×100 ml). Combined organic layer was washed with saturated sodium carbonate solution (3×100 ml). Aqueous carbonate layer was separated and acidified with 50% HCl solution and extracted with dichloromethane (3×100 ml). Combined organic layer was washed with brine solution (100 ml), dried over sodium sulfate and evaporated to yield Ethyl 2-cyano-3-hydroxy-but-2-enoate (58 g).

1. stirringstirred solution during 2 to 3 hours at ambient temperature
2. customReaction mixture
3. stirringwas stirred at ambient temperature for 15 to 20 hours
4. customReaction mixture
5. extractionextracted with dichloromethane (3×100 ml)
6. washCombined organic layer was washed with saturated sodium carbonate solution (3×100 ml)
7. customAqueous carbonate layer was separated
8. extractionextracted with dichloromethane (3×100 ml)
9. washCombined organic layer was washed with brine solution (100 ml)
10. dry with materialdried over sodium sulfate
11. customevaporated

ORD record

ord-a767062a5dc24eb999369bc291fb0787

Source dataset

uspto-grants-2013_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08389757B2