HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → Dibenzyl ethoxycarbonylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Dibenzylphosphite | HCID 21904359 | — |
| Reactant | Sodium dibenzylphosphite | HCID 23706462 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Dibenzyl ethoxycarbonylphosphonate | HCID 23320149 | — |
Reaction Steps
Ethanol (4.6 g) was added to a fine suspension of sodium metal (2.25 g) in dry ether (200 ml) under an atmosphere of nitrogen. The mixture was heated for 8 hours, after which dibenzylphosphite (25.7 g) in dry ether (50 ml) was added. After standing over-night the dibenzylphosphite sodium salt was added over a period of 2 hours to a cold solution of ethyl chloroformate (10.8 g) in ether, under an atmosphere of nitrogen. The reaction was heated at reflux for 1 hour, cooled, washed with water, a NaCl solution and dried over Na2SO4. The ether was evaporated. After evaporating and discarding components volatile at 0.01 mm and 150° C. the residue was collected (13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04386081 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-62d4fc39e053405f8402d6657e97658d |
| Source note | uspto-grants-1983_05 |