HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485069Generated: October 30, 2026
Dimethylformamide → 4-(difluoromethoxy)-3,5-dimethylbenzaldehyde
https://huagongshe.com/reaction/1485069
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Dimethyl-4-hydroxybenzaldehyde | HCID 75222 | — |
| Reactant | Sodium chlorodifluoroacetate | HCID 2734985 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(difluoromethoxy)-3,5-dimethylbenzaldehyde | HCID 2120281 | 94.9% |
Reaction Steps
To a mixture of 4-hydroxy-3,5-dimethylbenzaldehyde (2.00 g), N,N-dimethylformamide (54.0 mL) and water (6.00 mL), sodium chlorodifluoroacetate (6.09 g) and potassium carbonate (3.68 g) were added and the mixture was stirred at 120° C. for 4.5 hours. After cooling the reaction mixture to room temperature, water was added to it and two extractions were conducted with ethyl acetate. The combined organic layers were washed with water four times and thereafter washed with saturated brine. After drying over anhydrous magnesium sulfate, the desiccant was removed by filtration and the filtrate was then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=97:3-88:12) to give the titled compound as a colorless solid (2.53 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09422240B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-668bfcda6a354697b6778098f28d5cf7 |
|---|
| Source note | uspto-grants-2016_08 |
|---|