HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Cyanophenethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(2-Hydroxyethyl)benzonitrile | HCID 2800815 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyanophenethyl methanesulfonate | HCID 22632648 | — |
Reaction Steps
Methanesulfonyl chloride (18.6 g, 164 mmol) was added to a stirred solution of 4-(2-hydroxyethyl)benzonitrile (20 g, 136 mmol) and triethylamine (20.6 g, 204 mmol) in DCM (200 mL) at 0° C. The reaction mixture was stirred at rt until the reaction was complete (as indicated by tlc). Water (200 mL) was added and the organic layer was separated, dried and concentrated to give the sub-title compound in a quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559143B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-00418e4321884f2c98729d837f26b18e |
| Source note | uspto-grants-2003_05 |