HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889239Generated: October 28, 2026
Benzyl Alcohol → 1-(Benzyloxy)-3-fluoro-2-nitrobenzene
https://huagongshe.com/reaction/889239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Difluoro-2-nitrobenzene | HCID 87922 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Benzyloxy)-3-fluoro-2-nitrobenzene | HCID 57834982 | — |
Reaction Steps
A mixture of 1,3-difluoro-2-nitrobenzene (1.0 g, 6.29 mmol), benzyl alcohol (0.81 mL, 7.86 mmol) and potassium carbonate (1.74 g, 12.6 mmol) in DMF (5 mL) is heated at 60° C. for 18 h. The reaction mixture is poured into EtOAc, and washed with water and brine. The organic phase is concentrated and purified to give the title compound: 1H NMR (CDCl3) 7.36 (m, 6H), 6.83 (m, 2H), 5.20 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252820B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-19a3c7b7e2994e828b95d7cc43d3d618 |
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| Source note | uspto-grants-2012_08 |
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