HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → HCID 21667321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | HCID 21667313 | HCID 21667313 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 21667321 | HCID 21667321 | — |
Reaction Steps
By reaction of the 2-formylamino-3-hydroxy-4-phenyl-4-pentenoic acid methyl ester with thionyl bromide and subsequent treatment with triethyl phosphite in a manner analogous to that described in Example 1, and after chromatography (silica gel; ethyl acetate/hexane 4:1), E-2-formylamino-4-phenyl-5-diethylphosphono-3-pentenoic acid methyl ester is obtained in the form of a colourless oil. 1H-NMR (CDCl3): 2.98 (d, 2H,C(5)-H); 5.03 (dd, 1H, C(2)-H); 5.77 (dd, 1H, C(3)-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05175344 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-c4f92f8107314c9799494d83be66f483 |
| Source note | uspto-grants-1992_12 |