HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl phosphite → Dimethyl (Phthalimidomethyl)Phosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)- | HCID 79244 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Dimethyl (Phthalimidomethyl)Phosphonate | HCID 2773790 | 65% |
Reaction Steps
A mixture of N-(bromomethyl) phthalimide (i) (10.43 g, 43.46 mmol) and trimethyl phosphite (5.93 g, 47.80 mmol) was heated at reflux in xylene (20 mL) for 6 h. The reaction mixture was then cooled to room temperature and concentrated. Crystallization from CHCl3-hexane gave (ii) (7.60 g, 65%) as a white solid: 1H NMR (300 MHz, CDCl3) δH 3.84 (d, JH,P=10.8 Hz, 6 H), 4.12 (d, J=11.4 Hz, 2 H), 7.76 (m, 2 H), 7.87 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030103B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-984c6f2285c646758a4e24a205a7edb6 |
| Source note | uspto-grants-2006_04 |