HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Heptanoate → Dimethyl (2-oxooctyl)phosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Heptanoate | HCID 7797 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Dimethyl (2-oxooctyl)phosphonate | HCID 13390134 | — |
Reaction Steps
n-Butyllithiium (130 ml. of 1.6 M. solution) is slowly added to a solution of dimethyl methylphosphonate (25.6 g.) in 475 ml. of tetrahydrofuran (THF) at about -65° C. To the mixture is added a solution of ethyl heptanoate (18.4 g.) in 50 ml. of THF, annd the resulting mixture is stirred at about -70° C. for 2 hrs. Then, 16 ml. of acetic acid is added, and the mixture is concentrated under reduced pressure. The residue is mixed with dichloromethane (about 400 ml.) and water (about 50 ml.) shaken, and separated. The organic phase is dried over magnesium sulfate and concentrated. Distillation yields the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04130721 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-c2faf03a3fe7473386599f958ca774fd |
| Source note | uspto-grants-1978_12 |