HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1-(2-Fluoro-4-nitrophenyl)-4-imidazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,2-Difluoro-4-nitrobenzene | HCID 123053 | — |
| Reactant | 4-Imidazolidinone | HCID 1502063 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-Fluoro-4-nitrophenyl)-4-imidazolidinone | HCID 21026219 | 78.5% |
Reaction Steps
A solution of 4-imidazolidinone (9.5 g, 110.5 mmol), 3,4-difluoro nitrobenzene (12.2 ml, 110.5 mmol) and diisopropyl ethylamine (28.6 ml, 165 mmol) in dry DMF (80 ml) was heated to 60° C. overnight under argon. The reaction mixture was allowed to cool to room temperature and ice pieces were added. The solid formed was filtered and washed with water. The solid was dried under air to yield the nitro compound (19.5 g, 78.5%) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160912B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-c5f741b1b7e34f718d8b3fb9c77e992b |
| Source note | uspto-grants-2007_01 |