Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | 1,1,1-Trifluoro-2,4-pentanedione | HCID 73943 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18782298 | HCID 18782298 | — |
Reaction Steps
A mixture of 28.4 g (0.23 mol) of o-anisidine and 43.18 g (0.28 mol) of 1,1,1-trifluoro-2,4-pentanedione is heated at 100-105° C. for one hour and then cooled and the reaction medium is taken up with ethyl ether. 10 ml of 1 N hydrochloric acid are added. The mixture is filtered to remove the insoluble product, and the filtrate is concentrated under reduced pressure to give the expected product in the form of a beige solid (yield=98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06071917 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-048ac87bfb9e442b950e7bfe53f009ac |
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| Source note | uspto-grants-2000_06 |
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