HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 3-fluoro-N-(4-methoxybutyl)-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Difluoro-2-nitrobenzene | HCID 87922 | — |
| Reactant | 4-Methoxybutan-1-amine hydrochloride | HCID 45792349 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-fluoro-N-(4-methoxybutyl)-2-nitroaniline | HCID 58355413 | 66.6% |
Reaction Steps
To a solution of 1,3-difluoro-2-nitrobenzene (3.00 g) and diisopropylethylamine (7 μl) in acetonitrile (30 ml) was added a solution of 4-methoxybutan-1-amine hydrochloride (2.51 g) in acetonitrile (10 ml), and the mixture was stirred at room temperature for 90 hr. The reaction mixture was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (2:98-25:75) was concentrated under reduced pressure to give the object product (2.90 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045436B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-bc983d18b8334adc95aeaf693a102318 |
| Source note | uspto-grants-2015_06 |