HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → Diethyl (3-ethylisoxazol-5-yl)-methanephosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 5-(Chloromethyl)-3-ethyl-1,2-oxazole | HCID 12364600 | — |
| Product | Diethyl (3-ethylisoxazol-5-yl)-methanephosphonate | HCID 12520068 | 71.5% |
Reaction Steps
15 g of 5-chloromethyl-3-ethyl-isoxazole and 18 g of triethyl phosphite are slowly heated to 150° C. and left at this temperature for 21/2 hours. After the mixture has cooled, it is distilled under reduced pressure. 18.2 g of (3-ethylisoxazol-5-yl)-methanephosphonic acid diethyl ester of boiling point 120°-121° C./0.2 mm Hg are obtained. Yield: 71.2%. 1H-NMR spectrum (CDCl3, with TMS as internal standard): τ=3.85 (d, J=3 Hz, 1H), 4.17 (m, J=Hz, 4H), 6.60 (d, H=20 Hz, 2H), 7.35 (q, J=Hz, 2H), 8.50-8.93 (m, 9H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251539 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-dc104682bbd94ab0860d0fec1ee931ec |
| Source note | uspto-grants-1981_02 |