HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Dimethyl(2-oxo-4-phenylbutyl)phosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Ethyl 3-phenylpropionate | HCID 16237 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Dimethyl(2-oxo-4-phenylbutyl)phosphonate | HCID 2733973 | — |
Reaction Steps
A solution of dimethyl methylphosphonate (115.5 g.) in 2.1 l. of tetrahydrofuran is treated, while stirring at -65° C., with a solution of butyl lithium (660 ml. 1.6 M. in hexane). A solution of ethyl hydrocinnamate (93.5 g.) in 225 ml. of tetrahydrofuran is added at -65° C. Stirring is continued at -65° C. for 2 hrs. and then at about 25° C. for 16 hrs. Acetic acid (70 ml.) is added and the mixture concentrated under reduced pressure. The residue is partitioned between dichloromethane and water. The organic phase is dried and concentrated. Distillation yields the title compound, b. 188°-191° C./2 mm., having a mass spectral peak at 256.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04095036 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-6cddf40a71254a4dbb1287b462af38a1 |
| Source note | uspto-grants-1978_06 |