HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-(4-Methoxyphenyl)-2-trifluoromethylpropionitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 1-Chloro-1-(4-methoxyphenyl)-1-trifluoromethylethane | HCID 13885600 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Methoxyphenyl)-2-trifluoromethylpropionitrile | HCID 13885601 | 93% |
Reaction Steps
Trimethylsilyl cyanide (65.1 ml; 423 mmol) was added at room temperature to 1-chloro-1-(4-methoxyphenyl)-1-trifluoromethylethane (77.6 g; 335.5 mmol) in methylene chloride (975 ml) followed by titanium tetrachloride (32.5 ml; 3.25 mmol). After stirring for 20 hours at room temparature, 2N sodium hydroxide was added carefully, dropwise, until the mixture was neutral and the precipitate separated over celite. The aqueous phase was extracted with ethyl acetate and the extract dried over sodium suphate. After concentrating, there was obtained 2-(4-methoxyphenyl)-2-trifluoromethylpropionitrile (71.49 g=90% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791123 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-0985a8a20a6845289122f17cfb693fd6 |
| Source note | uspto-grants-1988_12 |