Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 18548215 | HCID 18548215 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18548198 | HCID 18548198 | — |
Reaction Steps
A solution of 3.8 mmol of 1-(7-hydroxyheptyl)-cyclopropene in 50 ml of ether was cooled in an ice bath. Triethylamine (1 ml) and 0.48 g of methanesulfonyl chloride (4.2 mmol) were added and the reaction mixture was stirred for 2½ hours at 0° C. The reaction mixture was washed with water and brine, dried over magnesium sulfate, filtered and stripped to give 1-(7-methanesulfonyloxyheptyl)-cyclopropene which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06365549B2 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-4a20151fb6b640deb3002cf5aa6780a2 |
|---|
| Source note | uspto-grants-2002_04 |
|---|