HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl vinyl ether → 2-Bromo-4-(1-ethoxy-ethoxy)-but-1-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | 3-Bromo-3-buten-1-ol | HCID 533975 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromo-4-(1-ethoxy-ethoxy)-but-1-ene | HCID 18548207 | 91.6% |
Reaction Steps
While cooling a solution of 10.38 g (0.0687 mol) of 3-bromo-3-buten-1-ol in 20 ml of diethyl ether with 50 mg (0.000263 mol) p-toluene sulfonic acid monohydrate in an ice water bath, 19 ml (0.199 mol) of ethyl vinyl ether was added slowly dropwise to maintain an internal temperature of <10° C. After 1 hour at 0° C., a few drops of triethylamine was added. The reaction mixture was poured onto water. The resulting mixture was transferred to a separatory funnel and the phases were separated. The isolated organic layer was washed with brine then dried over potassium carbonate and filtered. The solvent was removed from the filtrate in vacuo to yield 14.04 g of 2-bromo-4-(1-ethoxy-ethoxy)-but-1-ene as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548448B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-76ebaf9507254ae199d91d59c0e642b1 |
| Source note | uspto-grants-2003_04 |