HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → N-Isopropyl-4-fluoro-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | 4-Fluoro-2-nitroaniline | HCID 67769 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | N-Isopropyl-4-fluoro-2-nitroaniline | HCID 2775219 | 58% |
Reaction Steps
4-fluoro-2-nitroaniline (15.6 g; 0.1 mole), 2,2-dimethoxypropane (24.6 ml; 0.2 mole) and trifluoroacetic acid [TFA] (23.1 ml; 0.005 moles) were dissolved in toluene (500 ml) and stirred for 1 hr. BH3 * pyridine (10.0 ml; 0.1 moles) was added in 1.0 ml increments. The reaction was exothermic, and the reaction progress was monitored by tlc 40% EtOAc/Hexane. Additional TFA, BH3 * pyridine and 2,2-dimethoxypropane were added until the tlc indicated that the 4-fluoro-2-nitroaniline was consumed. The reaction mixture was placed on a bed of silica and eluted with 10% methyl-t-butylether/hexane. The product was the first major component to elute, which produced 11.2 g (58%) of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521193 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-060075e22e5747879ee58c6705373a56 |
| Source note | uspto-grants-1996_05 |