HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → 2-Methoxy-4,6-dimethylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 591070 | HCID 591070 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Methoxy-4,6-dimethylbenzaldehyde | HCID 13237473 | 89% |
Reaction Steps
Dimethylsulfate (16.4 g; 130 mmole) and potassium carbonate (20.7 g; 150 mmole) were added to a solution of 2,4-dimethyl-6-hydroxybenzaldehyde (20.0 g; 130 mmole) in acetone (200 ml). The mixture was heated under reflux with stirring for 48 hours and then evaporated to dryness. The residue was dissolved in dichloromethane and washed successively with water, aqueous sodium hydroxide (1M) and water, and then was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give 2,4-dimethyl-6-methoxybenzaldehyde (18.9 g; 89.0%). The product was obtained as a brown oil and was characterized by its proton magnetic resonance spectrum, the details of which are recorded in Table 2 below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806141 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-7cd7d6eee54f4e5097735b918ef06ccc |
| Source note | uspto-grants-1989_02 |