HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-2-fluoro-1-(trifluoromethoxy)benzene → 3-Fluoro-4-(trifluoromethoxy)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-2-fluoro-1-(trifluoromethoxy)benzene | HCID 2782217 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-Fluoro-4-(trifluoromethoxy)benzonitrile | HCID 17750670 | — |
Reaction Steps
49 g 1-Bromo-3-fluoro-4-trifluoromethoxybenzene was stirred into 100 mL dimethylacetamide together with 20 g copper(I)cyanide at 140° C. overnight. Additional 10 g copper cyanide was added and heating was continued at 150° C. for 4 h. Further 12 g copper cyanide was added and stirring continued at 150° C. overnight. After cooling, the mixture was filtered through Celite/Cellulose and washed with ethyl acetate. The filtrate was added to ice water and filtered again through Celite/Cellulose. The filtrate was extracted with ethyl acetate (×3), dried over magnesium sulfate and concentrated to provide a brown oil which was distilled at 7 mbar and 60° C. to yield two product fractions with 23.5 g and 12 g (content 80%) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187478B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-002ad2f0bf52484c95d6837d8e6b3a76 |
| Source note | uspto-grants-2015_11 |