HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,1,2-Tribromo-2-(2-benzenesulfonyloxyethyl)cyclopropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 1,1,2-Tribromo-2-(2-hydroxyethyl)cyclopropane | HCID 18548208 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1,2-Tribromo-2-(2-benzenesulfonyloxyethyl)cyclopropane | HCID 86586934 | 80% |
Reaction Steps
While cooling a solution of 3.00 g (0.00929 mol) of 1,1,2-tribromo-2-(2-hydroxyethyl)cyclopropane in methylene chloride with 0.901 ml (0.0111 mol) pyridine to 0° C., 1.18 ml (0.00929 mol) of benzene sulfonyl chloride was added dropwise via pipet. Allowed to warm to room temperature. After 3 days, water was added. The resulting mixture was transferred to a separatory funnel and the phases were separated. The organic layer was dried over MgSO4 and filtered. The solvent was removed from the filtrate in vacuo to yield 3.10 g of 80% pure 1,1,2-tribromo-2-(2-benzenesulfonyloxyethyl)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-a591de9f244b4a9aacb904d9fac8f0a0 |
| Source note | uspto-grants-2003_04 |