HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → alpha-Cyano-m-phenoxybenzyl mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)- | HCID 93218 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha-Cyano-m-phenoxybenzyl mesylate | HCID 20482835 | — |
Reaction Steps
α-Cyano-m-phenoxybenzyl alcohol (8.5 g, 38 mmol) is dissolved in 150 ml ether and cooled in an ice-bath. To the solution is slowly added methanesulfonyl chloride (5.4 g, 47 mmol) in 20 ml ether. After stirring about 20 minutes, triethylamine (4.76 g, 47 mmol) in 20 ml ether is added slowly and the mixture kept at 0° for 24 hours. Water is then added and the organic layer is separated, washed with 30% aqueous sodium bisulfite and water, dried and solvent removed under vacuum to yield α-cyano-m-phenoxybenzyl mesylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04178293 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-4dc89480c73b4080a08d017d6646be56 |
| Source note | uspto-grants-1979_12 |