HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexylamine → 2-Fluoro-n-hexyl-4-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,2-Difluoro-4-nitrobenzene | HCID 123053 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Fluoro-n-hexyl-4-nitroaniline | HCID 598056 | 91% |
Reaction Steps
To a solution of 3,4-difluoronitrobenzene (3.18 g, 20 mmol) in EtOAc (50 mL) were added Et3N (2.43 g, 24 mmol) and hexan-1-amine (2.02 g, 20 mmol). The reaction mixture was refluxed overnight, then cooled to rt and concentrated in vacuo to give the title compound as yellow oil (4.37 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434695B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-2ba673d1d82046bf98c0437cb95eb1a4 |
| Source note | uspto-grants-2016_09 |