HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Difluoromethoxy-6-propylsulfanylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromodifluoromethane | HCID 62407 | — |
| Reactant | 2-Hydroxy-6-propylsulfanylbenzonitrile | HCID 68566992 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Difluoromethoxy-6-propylsulfanylbenzonitrile | HCID 68565116 | — |
Reaction Steps
10.8 g (56 mmol) of 2-hydroxy-6-propylsulfanylbenzonitrile were dissolved in 120 ml of dimethylformamide, and 15.5 g (0.11 mol) of anhydrous potassium carbonate were added. Then, at room temperature, 8.2 g of bromodifluoromethane were passed in, and the mixture was stirred at room temperature for 5 hours. Then 15.5 g (0.11 mol) of anhydrous potassium carbonate and 7.2 g of bromodifluoromethane were added, and the mixture was stirred at room temperature overnight. The reaction mixture was worked up by pouring into water and extracting twice with methyl tert.-butyl ether. The organic phase was separated, washed several times with water and concentrated. The solid has been dried in vacuo at 50° C. Yield: 12.3 g of an oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07563921B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-8e25aa662d4b4dae9d49c8245bd9d31e |
| Source note | uspto-grants-2009_07 |