HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Cyano-2,5-difluorobenzyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2,5-Difluoro-4-(hydroxymethyl)benzonitrile | HCID 21904653 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyano-2,5-difluorobenzyl methanesulfonate | HCID 21904624 | — |
Reaction Steps
To an ice cooled solution of 2,5-difluoro-4-hydroxymethylbenzonitrile (3.10 g, 0.0183 mol; see step (iii) above) and methanesulfonyl chloride (2.21 g, 0.0192 mol) in 60 mL of methylene chloride was added triethyl amine (1.95 g, 0.0192 mol) with stirring. After 1.5 h at 0° C. the mixture was washed with water, dried (Na2SO4) and evaporated. The product could be used without further purification. Yield: 4.5 g (99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129233B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-477de7c5fb014f44bbca10576191d5ab |
| Source note | uspto-grants-2006_10 |