HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Fluoro-4-vinylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-(4-Cyano-3-fluorophenyl)ethyl methanesulfonate | HCID 86647309 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Fluoro-4-vinylbenzonitrile | HCID 21904607 | — |
Reaction Steps
A solution of 2-(4-cyano-3-fluorophenyl)ethyl methanesulfonate (35.0 g, 144 mmol) and triethylamine (50 mL) in DCM (200 mL) was added DBU (50 mL) dropwise to at 0° C. After stirring at room temperature overnight, the solution was diluted with DCM, washed with 1 N HCl and brine, and dried over anhydrous sodium sulphate and concentrated. The residue was purified by column chromatography to give title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206199B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-5114ddd5f6e34238904340d310b7f752 |
| Source note | uspto-grants-2015_12 |