HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2-(Difluoromethoxy)-6-fluorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Fluoro-6-hydroxybenzonitrile | HCID 2783216 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(Difluoromethoxy)-6-fluorobenzonitrile | HCID 23448361 | — |
Reaction Steps
6.3 g of chlorodifluoromethane were passed into a stirred mixture of 10.0 g of 2-hydroxy-6-fluorobenzonitrile, 50 ml of 1,2-dimethoxyethane and 25 ml of NaOH (33%) at 75° C. (the reflux condenser was cooled with dry ice), and stirring was continued for one hour at 70-75° C. After cooling, the batch was diluted with 300 ml of water and extracted three times using in each case 150 ml of tert-butyl methyl ether. After the solvent had been vaporated, 6.5 9 of the desired product were obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509501B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-544bef124c6e4dc2a36103e2682dc07e |
| Source note | uspto-grants-2003_01 |