HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3-Trifluoromethylphenylthioacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | 3-(Trifluoromethyl)benzenethiol | HCID 136751 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Trifluoromethylphenylthioacetonitrile | HCID 18543801 | — |
Reaction Steps
To sodium (0.62 g, 27.0 mmol) dissolved in 40 mL of ethanol was added 4.79 g (26.9 mmol) of 3-trifluoromethylthiophenol and 2.04 g (27.0 mmol) of chloroacetonitrile. The reaction mixture was heated at reflux for 1 hour and then stirred overnight at room temperature. To the cooled reaction mixture was added one volume of ether and the precipitated solids were removed by filtration. The filtrate was evaporated on the rotary evaporator to give the product as an oil in essentially quantitative yield. This material was used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06005109 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-aa62c2f81f7b4bba8b726abe0869c232 |
| Source note | uspto-grants-1999_12 |