HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513005Generated: October 26, 2026
Hydrochloric Acid → 5-Chloro-2-(2,3-difluoro-6-methoxybenzyloxy)-4-nitrophenol
https://huagongshe.com/reaction/1513005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Difluoro-6-methoxybenzyl bromide | HCID 4995861 | — |
| Reactant | 4-Chloro-5-nitrocatechol | HCID 12873364 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Chloro-2-(2,3-difluoro-6-methoxybenzyloxy)-4-nitrophenol | HCID 59309849 | 97.5% |
Reaction Steps
To a solution of 4-chloro-5-nitrocatechol (10.4 g) in N,N-dimethylformamide (55 mL) was added sodium hydride (55%, 5.04 g) under ice-cooling, and the mixture was stirred at the same temperature for 10 minutes. To the reaction mixture was added N,N-dimethylformamide (11 mL), followed by adding a solution of 2,3-difluoro-6-methoxy-benzyl bromide (14.3 g) in N,N-dimethylformamide (22 mL) under ice-cooling, and the mixture was stirred at the same temperature for 10 minutes, and then stirred at room temperature for 1.5 hours. The reaction mixture was diluted with water. The mixture was poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=7/3−1/1) to give the title compound (18.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217069B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-5232a465ce844a38a03d462ab33565c0 |
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| Source note | uspto-grants-2012_07 |
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