HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl phosphite → Dimethyl (4-hydroxy-3-methoxy-5-methylbenzyl)phosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | Trimethyl(4-hydroxy-3-methoxy-5-methylbenzyl)ammonium iodide | HCID 20634507 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Dimethyl (4-hydroxy-3-methoxy-5-methylbenzyl)phosphonate | HCID 86585635 | 83% |
Reaction Steps
Trimethyl(4-hydroxy-3-methoxy-5-methylbenzyl)ammonium iodide (1 g, 3.0 mmol) was suspended in 8 ml xylene, trimethyl phosphite (0.52 ml, 4.4 mmol) was added dropwise and the resulting mixture was refluxed for 14 h. The solid formed was filtered and the solvent and excess of phosphite were evaporated under vacuum to yield dimethyl (4-hydroxy-3-methoxy-5-methylbenzyl)phosphonate as a viscous oil (0.64 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706698B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-391ab93039044ba0a2ab64e6470e1512 |
| Source note | uspto-grants-2004_03 |