Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| Reactant | 16814-09-8 | HCID 250285 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 2315017 | HCID 2315017 | 64.3% |
Reaction Steps
83 g of 3-nitrobenzoyl chloride in 150 ml of acetonitrile are added dropwise to a solution of 105 g of 2-aminopropane-2-phosphonic acid diethyl ester and 45 g of triethylamine in 300 ml of acetonitrile at 0° C., with good stirring. After completion of the addition, the mixture is stirred for a further 3 hours at 0° C.; it is then filtered and the solvent is distilled off in vacuo. The residue is purified by extraction by shaking with ether and aqueous 2 normal sodium carbonate solution. 99 g of 2-(3'-nitrobenzamido)propane-2-phosphonic acid diethyl ester of melting point 95°-96° C. are obtained. This product is reduced with hydrogen as indicated in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04026709 |
|---|
| Source dataset | uspto-grants-1977_05 |
|---|
| ORD ID | ord-7de45dbf64de4e6691075ceb17a79119 |
|---|
| Source note | uspto-grants-1977_05 |
|---|