HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1-(Bromomethyl)-4-ethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 4-Ethylbenzyl alcohol | HCID 13034 | — |
| Product | 1-(Bromomethyl)-4-ethylbenzene | HCID 12231560 | — |
Reaction Steps
A mixture of 4-ethylbenzyl alcohol (2.72 g, 20 mmol, purchased from Aldrich) and 50 ml of 47% hydrobromic acid (purchased from Wako Junyaku Kogyo) was stirred vigorously for 30 minutes at room temperature. The reaction mixture was extracted with hexane to give 3.98 g of 4-ethylbenzyl bromide as a colorless oil. Then to a hot solution (50° C.) of sodium cyanide (1.96 g, 40 mmol) in 20 ml of dimethyl sulfoxide was added the above 3.98 g of 4-ethylbenzyl bromide and the mixture was stirred for 3 hours at ambient temperature. To the resultant reaction mass was added water and extracted with hexane. The solvent was removed to give 2.70 g (yield: 93.1%) of 4-ethylphenylacetonitrile as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05589506 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-b7a4aa2101a8486097bbf0110b04964f |
| Source note | uspto-grants-1996_12 |