HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-methoxy-5-methylbenzeneacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic acid, 5-methoxy-m-tolyl- | HCID 39879 | — |
| Product | Ethyl 3-methoxy-5-methylbenzeneacetate | HCID 22600115 | 85% |
Reaction Steps
To a solution 3-methoxy-5-methylphenylacetic acid of (8.1 g; 0.045 mol; from step (iii) above) in EtOH (100 mL) was added H2SO4 (conc.), and the solution was left to stand for 40 hours. The reaction mixture was concentrated, and the crude product was partitioned between water and ether. The organic layer was washed with NaHCO3/aq and water, dried (Na2SO4), and evaporated to yield 8.0 g (85%) of the sub-title compound as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06255301B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-89a21fa3af634c839105420dc7d6f966 |
| Source note | uspto-grants-2001_07 |