HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578800Generated: November 3, 2026
Water → 2,3-Difluoro-6-(2-methoxyethoxy)benzaldehyde
https://huagongshe.com/reaction/578800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | 2,3-Difluoro-6-hydroxybenzaldehyde | HCID 21221031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,3-Difluoro-6-(2-methoxyethoxy)benzaldehyde | HCID 57565810 | — |
Reaction Steps
To a suspension of 2,3-difluoro-6-hydroxybenzaldehyde (0.63 g) and potassium carbonate (0.83 g) in N,N-dimethyl -formamide (4 mL) was added 2-methoxyethyl bromide (0.45 mL), and the mixture was stirred at room temperature for 3 days. The reaction mixture was poured into water, and the resulting mixture was extracted with diethyl ether. The extract was washed with water and brine successively, 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=85/15−60/40) to give 2,3-difluoro-6-(2-methoxyethoxy)benzaldehyde (0.62 g). This material was dissolved in tetrahydrofuran (6 mL). To the solution were added water (0.6 mL) and sodium borohydride (0.12 g), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with water, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to give the title compound (0.61 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040693B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-797434c58249482493af4cf06f2d50ad |
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| Source note | uspto-grants-2015_05 |
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