Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-Chloro-2-nitro-4-(trifluoromethoxy)aniline | HCID 26596607 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66937403 | HCID 66937403 | 99.9% |
Reaction Steps
Piperidine (1.2 mL) was added to 5-chloro-2-nitro-4-trifluoromethoxy-phenylamine (0.757 g, 2.94 mmol) in a sealed tube and the mixture was heated to 100° C. for 2 h. The mixture was cooled to 23° C., poured into water (50 mL) and extracted with EtOAc (3×80 mL). The combined organic layers were washed with brine (50 mL), dried, filtered, and concentrated under reduced pressure to yield the titled compound (0.900 g, 99.9%). MS (ESI/CI): mass calcd. for C12H14F3N3O3, 305.1; m/z found, 306.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865713B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-b527c1fc030148b08c61207301254125 |
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| Source note | uspto-grants-2014_10 |
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