HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl [4-(2-Bromoethyl)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | [4-(2-Bromoethyl)phenyl]acetic acid | HCID 20386065 | — |
| Product | Ethyl [4-(2-Bromoethyl)phenyl]acetate | HCID 54408832 | — |
Reaction Steps
A solution of [4-(2-bromoethyl)phenyl]acetic acid (48.6 g., 0.2 mole) and sulfuric acid (1.5 ml.) in ethanol (400 ml.) is boiled under reflux for 6 hours. About 300 ml. of the ethanol is removed by distillation at reduced pressure. The residue is diluted with 400 ml. of water. The oily ester is taken up in ether, washed with water and brine, and dried over magnesium sulfate. Evaporation of the ether leaves the title compound as an oil which can be purified by distillation in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04175203 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-5a3da39c189244cc961cb3d9f24c7c30 |
| Source note | uspto-grants-1979_11 |