HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265987Generated: October 31, 2026
Water → 2-(2-Benzenesulfonyloxyethyl)-cyclopropene
https://huagongshe.com/reaction/1265987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,1,2-Tribromo-2-(2-benzenesulfonyloxyethyl)cyclopropane | HCID 86586934 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Benzenesulfonyloxyethyl)-cyclopropene | HCID 86586935 | 70% |
Reaction Steps
A solution of 0.745 g (0.00150 mol) of 1,1,2-tribromo-2-(2-benzenesulfonyloxyethyl)-cyclopropane in 4 ml of diethyl ether was placed under a nitrogen atmosphere by use of a Firestone valve. While cooling to −78° C. in a dry ice/acetone bath, 23.45 ml (0.00450 mol) of 1.4 M methyl lithium in diethyl ether was added slowly via syringe. After 15 minutes warmed to 0° C. in an ice water bath then returned to −78° C. for about 30 minutes before 2 ml of water was added via syringe. 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 with a bath temperature under 20° C. to yield >0.155 g of 70% pure 2-(2-benzenesulfonyloxyethyl)-cyclopropene contaminated with 30% 1-(2-hydroxethyl)cyclopropene as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06548448B2 |
|---|
| Source dataset | uspto-grants-2003_04 |
|---|
| ORD ID | ord-588e9d0bad8d43e08b3aad58a7e3e515 |
|---|
| Source note | uspto-grants-2003_04 |
|---|