HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427860Generated: November 3, 2026
3,4-Dihydroxybenzaldehyde → 4-(Difluoromethoxy)-3-hydroxybenzaldehyde
https://huagongshe.com/reaction/2427860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium chlorodifluoroacetate | HCID 2734985 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Difluoromethoxy)-3-hydroxybenzaldehyde | HCID 2758295 | 44.3% |
Reaction Steps
Sodium hydroxide (4.8 g, 120 mmoles) is added to a solution of 3,4-dihydroxybenzaldehyde (16.6 g, 120 mmol) and sodium chlorodifluoroacetate (18.3 g, 120 mmol) in dimethylformamide (150 mL) and water (3 mL). The mixture is heated to 120° C. and stirred at this temperature for 2 hours. The solvent is removed by vacuum distillation and aqueous hydrochloric acid (20 mL) is added to the residue. The mixture is extracted with diethyl ether (2×50 ml), the combined organic layers are washed with water and brine and the solvent removed under reduced pressure. The crude product is purified by chromatography on silica gel (hexane/ethyl acetate 8:2) to furnish 4-difluoromethoxy-3-hydroxybenzaldehyde as a colourless solid (10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968724B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-6eb932ca148f40c8afdbece9b862f237 |
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| Source note | uspto-grants-2011_06 |
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