HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850429Generated: October 26, 2026
Dimethyl Sulfoxide → 3-Methoxy-2-(pentyloxy)benzaldehyde
https://huagongshe.com/reaction/850429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3-Methoxy-2-pentyloxyphenyl)methanol | HCID 19363470 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Methoxy-2-(pentyloxy)benzaldehyde | HCID 19363290 | 97.5% |
Reaction Steps
The crude product of (3-methoxy-2-pentyloxyphenyl)methanol (1.2 g), dimethyl sulfoxide (DMSO, 25 ml) and triethylamine (6.72 ml, 48.2 mmol) were mixed, and this solution was cooled to 0° C. Sulfur trioxide--pyridine complex (2.56 g, 16.1 mmol) was added, and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into water to stop the reaction, and the aqueous layer was extracted 3 times with ethyl acetate (30 ml). The organic layers were combined, washed with 2N hydrochloric acid (30 ml), water (30 ml) and saturated brine (30 ml), and dried over anhydrous magnesium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography (hexane/ethyl acetate=15/1-10/1) to give 3-methoxy-2-pentyloxybenzaldehyde (1.16 g, 83% in 3 steps) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06017919 |
|---|
| Source dataset | uspto-grants-2000_01 |
|---|
| ORD ID | ord-4619f26ca0ab42a5809218a8b39a7def |
|---|
| Source note | uspto-grants-2000_01 |
|---|