Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | 4-Nitroanilinium chloride | HCID 85156 | — |
| Reactant | Ethyl 3-(3-fluorophenyl)-3-oxopropanoate | HCID 2063904 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 69202260 | HCID 69202260 | 20.8% |
Reaction Steps
3-(3-Fluorophenyl)-3-oxo-propionic acid ethyl ester, 106.3 grams (0.506 moles), 4-nitro-aniline, 63.0 grams (0.456 moles), and 4-nitro-aniline hydrochloride 4.0 grams (0.023 moles) were placed in a dry 2 L round-bottom flask. To the mixture was added 1.3 L of n-butanol, the flask was fitted with a Soxhlet extractor (cup volume of 0.3 L), condenser and nitrogen inlet. Dry, activated 4 Å sieves (200 grams) were placed in the extractor cup and the reaction mixture heated to reflux at 118° C. under nitrogen and maintained at that temperature for 90 hours. The reaction mixture was decanted while hot from a small amount of solids and chilled to −15° C. for 48 hours Crystalline solids were collected by vacuum filtration. The crystals were washed with 0.2 L of cold ethanol and two 0.2 L portions of hexanes and vacuum dried at 50° C. overnight to yield 35.8 grams (20.8% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06815447B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-81cb8f7f8f6a4122ae8e19113514e362 |
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| Source note | uspto-grants-2004_11 |
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