HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzonitrile → HCID 178510095, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzonitrile | HCID 14517 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178522079 | HCID 178522079 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178510095 | HCID 178510095 | — |
Reaction Steps
To a solution of 07086 (1.35 g, 4 mmol) in DMF (40 mL) was added 60% sodium hydride in oil (0.24 g, 6 mmol) portionwise at 0° C. After 10 min, 4-fluorobenzonitrile (0.73 g, 6 mmol) was added. The reaction mixture was allowed to slowly warm to room temperature overnight. The reaction was quenched by adding water and the resulting white precipitates were collected and washed with water. The collected solid was recrystallized from methanol to give the title compound, 1.5 g (86%) as a white solid. 1H NMR (300 MHz, DMSO-d6): δ 8.83-8.78 (s, 1H), 8.08 (d, J=2 Hz, 1H), 7.75 (d, J=9 Hz, 2H), 7.57-7.47 (m, 2H), 7.13 (d, J=9 Hz, 2H), 6.37 (d, J=7 Hz, 1H), 4.55-4.41 (m, 1H), 3.62-3.43 (m, 1H), 2.15-1.83 (m, 4H), 1.60-1.30 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029401B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-d6113d848ea84099b550af7758d1bcb0 |
| Source note | uspto-grants-2015_05 |