Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-chlorophenoxy)-3-(trifluoromethyl)aniline | HCID 726092 | — |
| Reactant | HCID 54546667 | HCID 54546667 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20393504 | HCID 20393504 | 80.1% |
Reaction Steps
To a solution containing 2.9 g (0.01 mole) of the amine prepared in Example 4 (b), and 1.0 g (0.01 mole) of triethylamine in 50 ml of tetrahydrofuran was added dropwise 1.7 g (0.01 mole) of 1-butylcyclopropanecarboxylic acid chloride. The mixture was stirred and heated at 60° C. for 0.5 hour, poured into ice water and extracted with ether. The ether extract was dried and concentrated under reduced pressure. The residual yellow syrup was crystallized from hexane to give 3.3 g (80%) of product as a tan solid, m.p. 104°-106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04166735 |
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| Source dataset | uspto-grants-1979_09 |
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| ORD ID | ord-c74230c605c04a6780b03bce5248efb1 |
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| Source note | uspto-grants-1979_09 |
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