Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 1,2,4-Triacetoxybenzene | HCID 69169 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1,2,4-Benzenetriol | HCID 10787 | — |
Reaction Steps
Eighty grams of the crude 1,2,4-triacetoxybenzene were dissolved in 200 ml of methanol containing 6 g of concentrated sulfuric acid. The reaction mixture was boiled under reflux for one hour. Then the solution was cooled to room temperature and neutralized with an equivalent amount of fine powdered sodium carbonate. Thereafter 800 ml of ethylether was added whereupon sodium sulfate precipitated out, which was removed by filtration. Reaction by-products and contaminants being responsible for a dark red coloration may be removed employing solid silica gel. After evaporation of the supernatant under reduced pressure, a dark red oil is obtained which crystallized upon standing at 40° C. in the form of a slight reddish solid mass which is pure enough for the next step. This product is 1,2,4-trihydroxybenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04366082 |
|---|
| Source dataset | uspto-grants-1982_12 |
|---|
| ORD ID | ord-694ef1eba17d4e9eb9c518b1ed3fdd7a |
|---|
| Source note | uspto-grants-1982_12 |
|---|