HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → HCID 86740148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Fluazifop-P | HCID 91733 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 13055221 | HCID 13055221 | — |
| Product | HCID 86740148 | HCID 86740148 | — |
Reaction Steps
Following the above procedures, (R)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionic acid chloride, prepared from (R)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionic acid and thionyl chloride, is reacted with the sodium salt of ethyl acetoacetate to give ethyl (R)-2-acetyl-4-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]-3-oxopentanoate (XVIII: Q1 is N, Y is hydrogen, Z is trifluoromethyl and R3 is ethyl). This pentanoate is then heated with sodium chloride to give (R)-5-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]2,4-hexanedione (XIX; Q1 is N, Y is hydrogen and Z is trifluoromethyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04522647 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-bd398e64570343ba90febfa69bbbd91d |
| Source note | uspto-grants-1985_06 |