HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 4-[(5-Amino-1,3,4-oxadiazol-2-yl)methyl]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 2-(4-Hydroxyphenyl)acetohydrazide | HCID 3731866 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[(5-Amino-1,3,4-oxadiazol-2-yl)methyl]phenol | HCID 21919315 | — |
Reaction Conditions
| Temperature | 2.5 °C |
|---|
Reaction Steps
Solid BrCN 6.059 g (57.2 mmol) was added in one portion into ice-cooled slurry of (4-hydroxy-phenyl)-acetic acid hydrazide 8.642 g (52.0 mmol) and KHCO3 6.510 g (65 mmol) in MeOH (100 mL). The mixture was stirred at 0-5° C. for 1 hour, the ice bath allowed to melt and stirred at room temperature overnight (18 hr). The reaction mixture was diluted with water (100 mL), stirred for 1 hour, the precipitate was collected by filtration, washed with water and dried on high vacuum. A second fraction precipitated after concentrating and cooling the supernatants.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07037909B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-7b2aa49c5bc340b087a376f9edc1fc9b |
| Source note | uspto-grants-2006_05 |