HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279417Generated: October 31, 2026
Dimethyl Sulfoxide → 2-Formyl-3-benzyloxy-6-methyl-pyran-4(1H)-one
https://huagongshe.com/reaction/1279417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-hydroxymethyl-3-benzyloxy-6-methyl-pyran-4(1H)-one | HCID 11139409 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Formyl-3-benzyloxy-6-methyl-pyran-4(1H)-one | HCID 12011187 | 87.7% |
Reaction Steps
To a solution of 2-hydroxymethyl-3-benzyloxy-6-methyl-pyran-4(1H)-one (5.28 g, 21.5 mmol, 1 eq) in 100 ml chloroform was added 27 ml of dimethyl sulfoxide and 18.5 ml of triethylamine and the reaction mixture was cooled with an ice-bath to an internal temperature of 3-5° C. Then sulfur trioxide pyridine complex (17.1 g 107 mmol, 5 eq) was added and the mixture was allowed to thaw to room temperature. After stirring for overnight at room temperature, the reaction mixture was washed with water (2×50 ml) and the organic phase was dried over Na2SO4, filtered and concentrated in vacuo to yield an organe oil. Further purification by column chromatography on silica gel (eluant: Et2O) furnished the pure product (4.6 g, 87.7%) as a white crystalline solid. m.p. 78-81° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06448273B1 |
|---|
| Source dataset | uspto-grants-2002_09 |
|---|
| ORD ID | ord-a50e998f4b844593a593720baba50c65 |
|---|
| Source note | uspto-grants-2002_09 |
|---|