HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237288Generated: October 31, 2026
Benzyl Alcohol → 1-(Benzyloxy)-2,5-difluoro-4-nitrobenzene
https://huagongshe.com/reaction/2237288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2,4-Trifluoro-5-nitrobenzene | HCID 75012 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Benzyloxy)-2,5-difluoro-4-nitrobenzene | HCID 57470868 | 92% |
Reaction Steps
A mixture of 2,4,5-trifluoronitrobenzene (5.4 g, 30.8 mmol), benzylalcohol (3.2 mL, 30.8 mmol) and potassium carbonate (6.4 g, 46.1 mmol), in DMF (20 mL), was stirred at ambient temperature for 72 h. Water (60 mL) was added and the mixture was cooled at 4° C. for 24 h. The resultant precipitate was filtered, rinsed with water and dried in vacuo to afford the product (7.5 g, 92%) as a pale yellow solid. 1H NMR (CDCl3) δ 7.90-7.94 (m, 1H), 7.38-7.44 (m, 5H), 6.85-6.90 (m, 1H), 5.22 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07714138B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-fc3bbfcdae6b473e917ac8fd4688bce2 |
|---|
| Source note | uspto-grants-2010_05 |
|---|