HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → 5-Diethylphosphonomethyl-3-methylisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 5-(Chloromethyl)-3-methyl-1,2-oxazole | HCID 7131496 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Diethylphosphonomethyl-3-methylisoxazole | HCID 10585698 | — |
Reaction Steps
445 g of 5-chloromethyl-3-methylisoxazole and 674 g of triethyl phosphite are slowly heated to 150° C. and left at this temperature for 4 hours. After distillation, 546 g (69% of theory) of (3-methylisoxazol-5-yl)-methanephosphonic acid diethyl ester of boiling point 118°-121° C./0.3 mm Hg are obtained. 1H-NMR spectrum (CHCl3, with TMS as internal standard): τ=3.85 (d, J=3 Hz, 1H), 4.17 (m, J=8 Hz, 4H), 6.67 (d, J=22 Hz, 2H), 7.72 (s, 3H), 8.67 (t, J=8 Hz, 6H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251539 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-2328a7143ec24e42a9b5fb95f5334c5c |
| Source note | uspto-grants-1981_02 |