HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → HCID 20278413, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 20278422 | HCID 20278422 | — |
| Reactant | HCID 54519821 | HCID 54519821 | — |
| Product | HCID 20278413 | HCID 20278413 | — |
Reaction Steps
In the same manner, 2-[4-(6-trifluoromethyl-2-quinoxalinyloxy)phenoxy]propionic acid chloride is prepared from the corresponding propionic acid and oxalyl chloride, and is then reacted with the sodium salt of methylacetoacetate to give methyl 2-acetyl-4-[4-(6-trifluoromethyl-2-quinoxalinyloxy)phenoxy]-3-oxopentanoate (XIV; X' is CF3 and X" is hydrogen). The pentanoate is then heated with sodium chloride and DMSO to yield 5-[4-(6-trifluoromethyl-2-quinoxalinyloxy)phenoxy]-2,4-hexanedione (XV; X' is CF3 and X" is hydrogen).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04522647 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-d2f8ba1b331a49f095ab9c5954d86d23 |
| Source note | uspto-grants-1985_06 |