HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → 4-(Diethylamino)-3-(trifluoromethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Bromo-3-(trifluoromethyl)benzonitrile | HCID 10800647 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-(Diethylamino)-3-(trifluoromethyl)benzonitrile | HCID 68677448 | — |
Reaction Conditions
| Temperature | 135 °C |
|---|
Reaction Steps
A mixture of 4-bromo-3-(trifluoromethyl)-benzonitrile (Yonezawa et al., Synthetic Communications (1996), 26, 1575-1578; 6.0 g, 24 mmol), diethylamine (8.3 mL, 80 mmol) and 25 mL N,N-dimethylacetamide is stirred in a tightly closed vessel for 16 hours at 135° C. After cooling, the reaction mixture is treated with a half-saturated aqueous solution of sodium hydrogen carbonate and extracted three times with ethyl acetate. The combined organic extracts are dried (Na2SO4) and the solvent is evaporated off under reduced pressure. The crude product is purified by column chromatography on silica gel, eluent hexane/ethyl acetate to give the title compound as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07655669B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-dece2e21328944b8b1c8f36a9cc25562 |
| Source note | uspto-grants-2010_02 |