Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Methylanisole | HCID 7731 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Methylanisole | HCID 7731 | — |
| Product | 4-Methoxybenzaldehyde | HCID 31244 | — |
Reaction Steps
Into the same flask as in Example 1 are placed 400 ml of water, 87 g of sulfuric acid, 5 g of manganic sulfate and 100 g of p-methoxytoluene, and the mixture is stirred. Into a 1-liter beaker are placed 540 ml of water, 86 g of chromic anhydride and 246 g of sulfuric acid to prepare an oxidizing solution. The oxidation process of Example 2 is repeated in the same manner except that the reaction temperature is maintained at 80° C for 21/3 hours. The reaction mixture is treated in the same manner as in Example 1, affording 70 g of anisaldehyde, 27 g of unreacted p-methoxytoluene and 5 g of the residue. Conversion 73%. Yield 86%. Aldehyde selectivity 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04297520 |
|---|
| Source dataset | uspto-grants-1981_10 |
|---|
| ORD ID | ord-de53053a72e44066b382014d1cb7aeb9 |
|---|
| Source note | uspto-grants-1981_10 |
|---|