HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → Ethyl 2-(4-formylphenoxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Product | Ethyl 2-(4-formylphenoxy)acetate | HCID 291358 | — |
Reaction Steps
p-Hydroxybenzaldehyde (4.88 g), bromoacetic acid (6.68 g) and potassium carbonate (5.53 g) were suspended in 100 ml of acetone, and refluxed for 15 hours. After the solvent was distilled off under reduced pressure, water was added followed by extraction with methylene chloride. The organic phase was washed in saturated aqueous sodium chloride, and dried over magnesium sulfate. After distillation of the solvent under reduced pressure, 8.32 g of ethyl 4-formylphenoxyacetate was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374641 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-d2cb29f612194fb1b1fc039a223d3422 |
| Source note | uspto-grants-1994_12 |