HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphonoacetate → Ethyl 3-(4-nitrophenyl)-3-phenylprop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methanone, (4-nitrophenyl)phenyl- | HCID 70839 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 3-(4-nitrophenyl)-3-phenylprop-2-enoate | HCID 308955 | — |
Reaction Steps
To a stirred suspension of sodium hydride, derived from 10.56 g. of a 50% suspension in mineral oil, in 400 ml. of 1,2-dimethoxyethane was added 51.6 g. of diethyl ethoxycarbonylmethylphosphonate, during 1 hour. When gas evolution ceased, a solution of 47.7 g. of 4-nitrobenzophenone in 400 ml. of 1,2-dimethoxyethane was added, dropwise, during 1.5 hours. Stirring was continued overnight and then the solvent was removed by evaporation in vacuo. The residue was partitioned between ethyl acetate and water. The layers were separated, and the water layer was extracted with fresh ethyl acetate. The combined ethyl acetate solutions were evaporated in vacuo to give the title compound as an oil, which slowly solidified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04342781 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-c2861430d7a84f4e9e63be0ff61640c3 |
| Source note | uspto-grants-1982_08 |