HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201784Generated: October 29, 2026
Acetic Acid → 3,5-Difluoro-4-formylbenzonitrile
https://huagongshe.com/reaction/2201784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3,5-Difluorobenzonitrile | HCID 587204 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Difluoro-4-formylbenzonitrile | HCID 16218256 | 42.1% |
Reaction Steps
To a solution of 3,5-difluorobenzonitrile (1 gm, 7.1 mmol) in dry tetrahydrofuran (20 mL), lithium diisopropylamide (0.769 gm, 7.1 mmol) was added at −78° C. The resulting reaction mixture was stirred for about 1 hour. Dimethylformamide (0.62 g, 8.5 mmol) was added dropwise to the reaction mixture and stirring was continued for about 45 minutes. Acetic acid (1.5 mL) and water (40 mL) were added to the cold solution of reaction mixture. The aqueous phase was extracted with diethyl ether (4×50 mL). The combined organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by silica gel (100-200) column chromatography using hexane and ethyl acetate as gradient system to afford pure 3,5-difluoro-4-formylbenzonitrile (0.5 gm, 31.25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09364466B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-effb54d589a949029c4dbf3b186042e4 |
|---|
| Source note | uspto-grants-2016_06 |
|---|