HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzoic Acid | HCID 243 | — |
Reaction Steps
Potassium permanganate (3.16 g, 0.02 mol) in water (35 ml) was stirred for 10 minutes and then cooled in a water bath while phenylacetonitrile or benzyl alcohol (0.011 mol), benzene (20 ml) and the catalyst (Table 5) (1mmol) were added. The mixture was stirred for 3 hours at room temperature and worked up by addition of 4% sodium bisulphite (60 ml), acidification with 2N hydrochloric acid, separation of organic layer and extraction of the aqueous layer with benzene (2×20 ml). The combined organic extracts were dried over magnesium sulphate and the solvent evaporated on a rotary evaporator. Recrystallization of the solid residue obtained gives pure benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880894 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-cc63c73f754d4a9d866e6dab28a7682e |
| Source note | uspto-grants-1989_11 |