HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl iodide → 4-Butoxy-2,6-dimethylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dimethyl-4-hydroxybenzaldehyde | HCID 591072 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 4-Butoxy-2,6-dimethylbenzaldehyde | HCID 21274190 | 92% |
Reaction Steps
1-Iodobutane (9.2 g; 50 mmole) and potassium carbonate (6.9 g; 50 mmole) were added to a solution of 2,6-dimethyl-4-hydroxybenzaldehyde (7.5 g; 50 mmole) in methyl ethyl ketone (150 ml). The mixture was heated under reflux with stirring for 20 hours and then evaporated to dryness. The residue was dissolved in dichloromethane and washed with water, then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give 4-butoxy-2,6-dimethylbenzaldehyde (9.4 g; 92.0%). The product was obtained as a yellow 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-179b738ace5042689b38d52d16fd7515 |
| Source note | uspto-grants-1989_02 |