HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-(2-Bromo-3-formylphenoxy)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-(2-Bromo-3-formylphenoxy)propanoic acid | HCID 86635922 | — |
| Product | Ethyl 3-(2-Bromo-3-formylphenoxy)propanoate | HCID 86635923 | — |
Reaction Steps
To a solution of 3-(2-bromo-3-formylphenoxy)propanoic acid from the previous step (I eq.) in EtOH (0.13 M) was added conc. sulfuric acid (0.8 eq.). The reaction was heated at reflux for 30 min. The reaction mixture was quenched with water and extracted with EtOAc. The combined organic extracts were washed with water and sat. aq. NaHCO3. Drying over Na2SO4, filtration and concentration of the filtrate in vacuo afforded the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063105B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-4eb173b7fb4341ba88696b8add55b4c1 |
| Source note | uspto-grants-2011_11 |