HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Benzyloxyphenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4-Benzyloxybenzyl chloride | HCID 70042 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Benzyloxyphenylacetonitrile | HCID 522804 | 95.7% |
Reaction Steps
In a 100 ml four-necked flask, there were placed 3.2 g of water, 1.23 g (0.025 mole) of sodium cyanide and 0.16 g of triethylbenzylammonium chloride, and a solution prepared by dissolving 5.3 g (0.023 mole) of 4-benzyloxybenzyl chloride in 6 g of benzene was further added thereto under stirring. Then, the resultant mixture was heated at a temperature of 80° C. for 5 hours under stirring to permit a reaction. After completion of the reaction, the formed organic layer is washed with water and dried over anhydrous sodium sulfate, followed by distilling off benzene to obtain 4.83 g (0.022 mole) of 4-benzyloxyphenylacetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04412082 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-bc8b17a29a6a467894d09da987b7a9d3 |
| Source note | uspto-grants-1983_10 |