HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (4-tert-Butylphenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene | HCID 87836 | — |
| Catalyst | Dibenzo-18-crown-6 | HCID 26541 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (4-tert-Butylphenyl)acetonitrile | HCID 76784 | 31.2% |
Reaction Steps
0.22 g of dibenzo-18-crown-6-ether and 1.57 g of sodium cyanide were suspended in 20 ml of DMSO, and 5.00 g of 4-tert-butylbenzyl bromide was dropwise added thereto with cooling with water. After having been stirred overnight at room temperature, the resulting mixture was further stirred at 50° C. for 5 hours. After this was left to be at room temperature, water was added thereto and extracted with ether. The organic layer was washed with water, and dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The residual product was purified through silica gel column chromatography to obtain 1.19 g of 4-tert-butylphenylacetonitrile was obtained from the fraction eluted with n-hexane:ethyl acetate=5:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566683B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-569f3bc130a64fa293f9f3ff2d40ee52 |
| Source note | uspto-grants-2009_07 |