HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl vinyl ether → 1-Bromo-2-(1-ethoxyethyl)oxymethyl-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | 2-Bromobenzyl alcohol | HCID 72850 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Bromo-2-(1-ethoxyethyl)oxymethyl-benzene | HCID 15483785 | 98.2% |
Reaction Steps
Pyridinium p-toluenesulfonate (0.50 g, 0.002 mol) was added to a mixture of 2-bromobenzylalcohol (18.70 g, 0.1 mol), dichloromethane (150 ml) and ethyl vinyl ether (14.42 g, 0.2 mol) under ice-cooling, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, half-saturated aqueous sodium bicarbonate solution (300 ml) was added, and the mixture was extracted with dichloromethane (100 ml) twice. The extracts were dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 1-bromo-2-(1-ethoxyethyl)oxymethylbenzene (25.44 g, yield: 98.2%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362212B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-788afae212e146e89ef312c7e97df4ca |
| Source note | uspto-grants-2002_03 |