HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-(4-Acetoxybutoxy)-5-hydroxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Butanol, 4-bromo-, 1-acetate | HCID 78491 | — |
| Reactant | 3,5-Dihydroxybenzaldehyde | HCID 94365 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Acetoxybutoxy)-5-hydroxybenzaldehyde | HCID 23143882 | 32.5% |
Reaction Steps
3,5-Dihydroxybenzaldehyde (0.96 g) and potassium carbonate (1.44 g) were suspended in N,N-dimethylformamide (5 mL). To the mixture was added 4-bromobutyl acetate (1.49 g) under ice-cooling, and the mixture was stirred at room temperature for 16 hours. To the reaction mixture was added 1 mol/L hydrochloric acid, and the resulting mixture was extracted with diethyl ether. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and brine successively and dried over anhydrous magnesium sulfate. The filtrate was concentrated under reduced pressure, and the obtained residue was purified by column chromatography on silica gel (ethyl acetate/hexane=1/5) to give the title compound (0.57 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547680B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-589be94f517b4c5b9467395164e3d3af |
| Source note | uspto-grants-2009_06 |