HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-[4-Chloro-3-(trifluoromethyl)phenyl]prop-2-enenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | 4-Chloro-3-(trifluoromethyl)benzaldehyde | HCID 118642 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[4-Chloro-3-(trifluoromethyl)phenyl]prop-2-enenitrile | HCID 54176226 | 87.1% |
Reaction Steps
A solution consisting of 10.6 g (0.06 mol) of diethyl cyanomethylphosphonate and 12.5 g (0.06 mol) of 4-chloro-3-trifluoromethylbenzaldehyde in 65 ml of tetrahydrofuran is added dropwise to a suspension of 6.7 g (0.12 mol) of powdered potassium hydroxide in 185 ml of tetrahydrofuran. During this process, there is a slight evolution of heat. Subsequently, the mixture is stirred at room temperature for 20 minutes and the solid material which separates off is filtered off and washed with tetrahydrofuran. The filtrate is concentrated in vacuo and the remaining residue is dried. 12.1 g (87.0% of theory) of 4-chloro-3-trifluoromethyl-cinnamonitrile are obtained as an E/Z isomeric mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428049 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-d4caff9d09254cf9a804c28ae2cf88db |
| Source note | uspto-grants-1995_06 |