HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Phenoxy-alpha-hydroxyiminobenzyl cyanide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butyl nitrite | HCID 10996 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Phenoxyphenylacetonitrile | HCID 141221 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Phenoxy-alpha-hydroxyiminobenzyl cyanide | HCID 85321215 | 78,002.102% |
Reaction Steps
85% Potassium hydroxide (3.96 g, 0.06 mol), toluene (100 ml) and butyl nitrite (6.19 g, 0.06 mmol) were added to 2-phenoxybenzyl cyanide (10.46 g, 0.05 mol). The mixture was stirred at room temperature for 16 hours. After completion of the reaction, water (100 ml) was added. The mixture was neutralized with hydrochloric acid, extracted with ether (150 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give 2-phenoxy-α-hydroxyiminobenzyl cyanide (11.15 g, Yield: 93.6%, E/Z=11/89).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05442063 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-110de0b657cf41fbb17c21902e05528b |
| Source note | uspto-grants-1995_08 |