HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → 4-Methoxy-3,5-dimethylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 2758574 | HCID 2758574 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxy-3,5-dimethylbenzaldehyde | HCID 2758573 | 94.7% |
Reaction Steps
The aldehyde was synthesized according to the procedure of Example 46, Step 1 using the alcohol from Step 2 (7.5 g, 45 mmol), oxalyl chloride (6.35 g, 50 mmol), dimethylsulfoxide (8.8 g, 100 mmol) and triethylamine (10.2 g, 110 mmol) and in methylene chloride (100 ml). There was obtained 7 g (92%) of the desired aldehyde which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06426360B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-e0086035a1674424834efe0944aee7f0 |
| Source note | uspto-grants-2002_07 |