HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → (4-tert-Butylphenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Tetrabutylammonium | HCID 16028 | — |
| Reactant | 1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene | HCID 87836 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-tert-Butylphenyl)acetonitrile | HCID 76784 | — |
Reaction Steps
A mixture consisting of 107 g p-tert.butylbenzyl bromide, 2 g tetra butyl-ammonium jodide and 37 g NaCN in 50 ml water was heated during 1 hour at 100° C. After cooling the reaction mixture, the organic layer was separated and distilled in vacuo with a yield of 78 g of the desired cyanide. Then this product was fractionated in vacuo. Yield of p-tert.butylbenzyl cyanide: 65 g (80%): boiling point: 118° C./0,7 kPa: nD =1,5110. This cyanide has a very strong odor which reminds one of algae, seaweed and ozone with ambergris-like, fatty and animal notes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04459224 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-af5034d7c5a44ebc89bd5ca9c40ceed5 |
| Source note | uspto-grants-1984_07 |