HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → Triethyl 4-phosphonocrotonate, mixture of isomers
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | Ethyl (E)-4-bromobut-2-enoate | HCID 5373944 | — |
| Product | Triethyl 4-phosphonocrotonate, mixture of isomers | HCID 5365783 | — |
Reaction Steps
Ethyl 4-bromocrotonate (7.0 mL) was added to triethylphosphite (9.9 mL) at 120 to 130° C. during 60 minutes periods. After the generation of ethyl bromide ceased, the reaction solution was stirred at the same temperature for 3 hours. After cooling, the resulting reaction solution was concentrated under reduced pressure. Then the residue was purified by distillation at 150 to 210° C. under reduced pressure (17 to 21 hPa) to give triethyl 4-phosphonocrotonate as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877953B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-1b7724c1078e4691bfc77b728110268c |
| Source note | uspto-grants-2014_11 |