HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → Phenyl [1-(p-tolylsulfonylamino)ethyl]phenylphosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Diphenyl phenylphosphonite | HCID 239038 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Phenyl [1-(p-tolylsulfonylamino)ethyl]phenylphosphinate | HCID 54172963 | 79% |
Reaction Steps
A mixture of 0.15 mole each of diphenyl phenylphosphonite, acetaldehyde, and p-toluenesulfonamide in 100 g of chlorobenzene is stirred and warmed at 103°-115° C. for 1 hr, and the solvent and by-product phenol are removed by concentration of the reaction mixture to 120° at 0.5 mm. Ether is stirred into the residue, causing separation of 49.4g (79% yield) of solid product. Recrystallization twice from chlorobenzene gives a white solid: mp 178°-181°; 31P nmr (DMSO-d6)- 37.7 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04032601 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-01c96d3c130a4e90a40e60e0bc6f3664 |
| Source note | uspto-grants-1977_06 |