HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl phosphite → HCID 86745087, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | HCID 21667294 | HCID 21667294 | — |
| Reactant | HCID 53930741 | HCID 53930741 | — |
| Product | HCID 86745087 | HCID 86745087 | — |
Reaction Steps
The starting material is manufactured as follows: Reaction of 2-methylene-pentanal with isocyanoacetic acid ethyl ester analogously to Example 1 yields 5-(penten-2-yl)-2-oxazoline-4-carboxylic acid ethyl ester. By hydrolysis of the 5-(penten-2-yl)-2-oxazoline-4-carboxylic acid ethyl ester in a manner analogous to that described in Example 15, 2-formylamino-3-hydroxy-4-propyl-4-pentenoic acid ethyl ester is obtained.Reaction of the 2-formylamino-3-hydroxy-4-propyl-4-pentenoic acid ethyl ester with thionyl bromide and subsequent treatment with trimethyl phosphite in a manner analogous to that described in Example 1 yields E-2-formylamino-4-propyl-5-dimethylphosphono-3-pentenoic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05051413 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-f1bc7050b45a4e40a5d28be628fcec47 |
| Source note | uspto-grants-1991_09 |