HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1,1,2-Tribromo-2-(2-hydroxyethyl)cyclopropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 1,1,2-Tribromo-2-[2-(1-ethoxy-ethoxy)ethyl]-cyclopropane | HCID 18548194 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,1,2-Tribromo-2-(2-hydroxyethyl)cyclopropane | HCID 18548208 | 88.2% |
Reaction Steps
To a slurry of 16.5 g (0.0418 mol) of 1,1,2-tribromo-2-[2-(1-ethoxy-ethoxy)-ethyl]-cyclopropane in 145 ml methanol and 40 ml water, was added 0.306 g (0.00161 mol) p-toluene sulfonic acid monohydrate and 145 ml 6M hydrochloric acid. After stirring at room temperature for 1 hour, the solvent was removed from the reaction mixture in vacuo. To the residue, there was added ethyl acetate and 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 MgSO4 and filtered. The solvent was removed from the filtrate in vacuo to yield 11.9 g of 1,1,2-tribromo-2-(2-hydroxyethyl)cyclopropane as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548448B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-de6cfb93a6d846e8bd7627cee35c3a8d |
| Source note | uspto-grants-2003_04 |