HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → HCID 86745092, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | HCID 86745093 | HCID 86745093 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86745092 | HCID 86745092 | — |
Reaction Steps
By reaction of 2-formylamino-3-hydroxy-4-benzyl-3-pentenoic acid ethyl ester with thionyl bromide and subsequent treatment with triethyl phosphite at 100° in a manner analogous to that described in Example 1, and after chromatography (silica gel; ethyl acetate), E-2-formylamino-4-benzyl-5-diethylphosphono-3-pentenoic acid ethyl ester is obtained in the form of a colourless oil, 1H-NMR (CDCl3): 2.45 (d, 2H, C(5)--H); 3.80 (s, 1H, CH2); 5.51 (m, 1H, C(3)--H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05051413 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-4099504d247147e19bd9e015ddb4fa50 |
| Source note | uspto-grants-1991_09 |