HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 3,5-Difluoro-4-(2-propynyloxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4,5-Trifluorobenzaldehyde | HCID 2776954 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,5-Difluoro-4-(2-propynyloxy)benzaldehyde | HCID 57445667 | 102% |
Reaction Steps
To 50 ml of acetonitrile were added 12 g of propargyl alcohol, 16 g of 3,4,5-trifluorobenzaldehyde and 15 g of potassium carbonate, and the mixture obtained was stirred at room temperature for 1 day. Then, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid and brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 20 g of 3,5-difluoro-4-(2-propynyloxy)benzaldehyde represented by the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714168B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-f6b365fa758a4b6282d372d4eb8767e1 |
| Source note | uspto-grants-2010_05 |