Potassium Hydroxide → Ethyl 2-benzylacrylate

A mixture of KOH (8.5 g) in ethanol (100 mL) was added at room temperature to benzylmalonic acid diethyl ester (40 g) in ethanol (80 mL) and the whole was stirred at room temperature overnight, then concentrated by evaporation, thereafter water (14 mL) was added and then the mixture was acidified in an ice bath with concentrated hydrochloric acid (12.6 mL). Partitioning between water and ether was carried out, the organic phase was dried and the ether was distilled off. Then, pyridine (26 mL), piperidine (1.22 g) and paraformaldehyde (3.56 g) were added to the residue. The mixture was heated in an oil bath (130° ) for 90 minutes, cooled, water (440 mL) were added and extraction was carried out 3 times with n-hexane (150 mL). The combined organic phases were washed with water, 1N HCl, water, saturated NaHCO3 solution and brine. The solution was dried (MgSO4) and evaporated to give the title compound as colourless oil (26 g, 85% yield). 1H NMR: 300 MHz spectrum consistent with proposed structure.

1. concentrationconcentrated by evaporation
2. additionwater (14 mL) was added
3. customthe mixture was acidified in an ice bath with concentrated hydrochloric acid (12.6 mL)
4. customPartitioning between water and ether
5. customthe organic phase was dried
6. distillationthe ether was distilled off
7. additionThen, pyridine (26 mL), piperidine (1.22 g) and paraformaldehyde (3.56 g) were added to the residue
8. temperatureThe mixture was heated in an oil bath (130° ) for 90 minutes
9. temperaturecooled
10. additionwater (440 mL) were added
11. extractionextraction
12. washThe combined organic phases were washed with water, 1N HCl, water, saturated NaHCO3 solution and brine
13. dry with materialThe solution was dried (MgSO4)
14. customevaporated

ORD 기록

ord-49234da53e6a40af95a400d09ad649e8

출처 데이터셋

uspto-grants-1995_05

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05416119