HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Methyl 4-(1-ethoxyethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | bismuth(III) bromide | HCID 82232 | — |
| Reactant | Methyl 4-(1-hydroxyethyl)benzoate | HCID 586417 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 4-(1-ethoxyethyl)benzoate | HCID 89580551 | 55% |
Reaction Steps
To the solution of ethanol (77 mg, 1.67 mmol) in perchloromethane (80 mL) was added bismuth(III) bromide (743 mg, 1.67 mmol), the mixture was stirred for 30 minutes at room temperature, the methyl 4-(1-hydroxyethyl)benzoate (300 mg, 1.67 mmol) was added, the mixture was stirred at room temperature for 12 hours. Then the mixture was concentrated and purified by column chromatography (silica gel, Petroleum ether/ethyl acetate=20:1) to give methyl 4-(1-ethoxy ethyl)benzoate (191 mg, 55%) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409865B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-366d626554ab459fa8f19e26ecee9cea |
| Source note | uspto-grants-2016_08 |