HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Methoxybenzoylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Methoxybenzoylacetonitrile | HCID 233398 | — |
Reaction Steps
A 25.0 g. portion of α-bromo-p-methoxyacetophenone is suspended in 125 ml. of ethanol. A solution of 16.0 g. of sodium cyanide in 75 ml. of water is added, using an ice-water bath to keep the temperature at 25°-30° C. The mixture is stirred for 45 minutes at room temperature. A total of 1.2 liters of water is added in 200 ml. increments with filtration through celite until no more precipitate forms. The filtrate is acidified to pH 5 with acetic acid. The solid is collected, washed with water, dried and recrystallized from benzene giving p-methoxybenzoylacetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04173650 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-1edd1f6c04144de49225fd4a46496de2 |
| Source note | uspto-grants-1979_11 |