HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 15052496, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 15052485 | HCID 15052485 | — |
| Product | HCID 15052496 | HCID 15052496 | — |
Reaction Steps
6 g of tetraethyl [(5-methyl-3-isoxazolyl)amino]-methylene-bis(phosphonate) was dissolved in 60 ml of acetic anhydride and heated under reflux overnight. The reaction solution was concentrated under reduced pressure, and the resulting syrup was formed into a chloroform solution. This was washed with water and dried, and then the solvent was removed by distillation. The residue was purified on a silica gel column (eluent: 0.5-2% ethanolchloroform) to give 5.2 g of tetraethyl [N-acetyl(5-methyl-3-isoxazolyl)amino]methylene-bis(phosphonate) as a pale yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04973576 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-901d8edb9c7b4396a5b384a141f5f456 |
| Source note | uspto-grants-1990_11 |