HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → Benzeneacetonitrile, 3,5-difluoro-a-hydroxy-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 3,5-Difluorobenzaldehyde | HCID 588160 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzeneacetonitrile, 3,5-difluoro-a-hydroxy- | HCID 19887192 | 85.7% |
Reaction Steps
Under stirring, 21 ml of a saturated aqueous solution of sodium bisulfite were added little by little to the mixture of 10.0 g of 3,5-difluorobenzaldehyde, 3.6 g of sodium cyanide and 15 ml of water. Upon the gradual addition, ice pieces were added at the same time to maintain the reaction temperature at 20°-30° C. The reaction mixture was stirred for 10 hours and then extracted with benzene. The resulting organic layer was washed with water, dried over anhydrous sodium sulfate and then concentrated under reduced pressure, whereby 10.2 g of crude 3,5-difluoromandelonitrile were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05131947 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-76398a2498144985876a9623fc7111b9 |
| Source note | uspto-grants-1992_07 |