HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrafluoroborate → HCID 59516937, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrafluoroborate | HCID 26255 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) | HCID 2735153 | — |
| Reactant | HCID 59517007 | HCID 59517007 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59516937 | HCID 59516937 | 100% |
Reaction Steps
After adding 3.62 g of trimethyloxonium tetrafluoroborate (hereinafter, “Me3O+BF4−”) to a solution of 8.59 g of 2-(2-fluoro-4,5-dimethoxyphenyl)-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]thioacetamide in 400 ml of dichloromethane under a nitrogen atmosphere, the mixture was stirred at room temperature for 15 hours. Saturated aqueous sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with dichloromethane. After washing the organic layer with saturated brine, it was dried over anhydrous sodium sulfate. The desiccating agent was filtered, and the filtrate was concentrated under reduced pressure to give the title compound (8.89 g, crude product) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816522B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-02b47fad7967452aaf9020e5ee3b3c5a |
| Source note | uspto-grants-2010_10 |