HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl phosphite → HCID 86745091, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | HCID 23181459 | HCID 23181459 | — |
| Product | HCID 86745091 | HCID 86745091 | — |
Reaction Steps
The starting material is manufactured as follows: Reaction of 3,3-dimethyl-2-methylene-butanal with isocyanoacetic acid ethyl ester in amanner analogous to that described in Example 1 yields 5-(3,3-dimethylbuten-2-yl)-2-oxazoline-4-carboxylic acid ethyl ester, which is hydrolysed analogously to Example 17 to 2-formylamino-3-hydroxy-4-tert.-butyl-4-pentenoic acid ethyl ester. Subsequent reaction with thionyl bromide followed by treatment with trimethyl phosphite analogously to Example 1 yields E-2-formylamino-4-tert.-butyl-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-ac14ab655c2f4f9bb928b5ad4be123fc |
| Source note | uspto-grants-1991_09 |