HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → HCID 19913165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 19913165 | HCID 19913165 | — |
Reaction Steps
4-Ethyl acetoxy benzaldehyde was prepared by the reaction of one mole of ethyl bromoacetate with one mole of 4-hydroxy benzaldehyde in the presence of one mole of anhydrous Potassium Carbonate in refluxing acetone. This precursor material was vacuum distilled after filtration and concentration of the reaction mixture. The precursor boiled in the range 138°-140° C. at 0.2 mbar and appeared as a slightly yellowish liquid which crystallized on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05084490 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-d0b5a1f4cf7d4c6b83356d6e6939551f |
| Source note | uspto-grants-1992_01 |