HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032859Generated: October 31, 2026
Vanillin → 1-(4'-Hydroxy,3'-methoxyphenyl)-4-phenoxy-1-butene-3-one
https://huagongshe.com/reaction/1032859
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | HCID 178468789 | HCID 178468789 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4'-Hydroxy,3'-methoxyphenyl)-4-phenoxy-1-butene-3-one | HCID 53858922 | 76.5% |
Reaction Steps
4-Hydroxy-3-methoxybenzaldehyde (2.1 g, 13.8 mMol) and 3-phenoxypropane-2-one triphenylphosphorane (2.8 g, 6.9 mMol) (prepared as described by LeCorre: C. R. Acad. Sci. Paris, 273 81 (1971)) are dissolved in 100 ml of toluene and warmed to reflux. After three hours, the solvent is evaporated and the residue is taken up in tHF. Sodium bisulfite (10.0 g) is dissolved in 100 ml of water and stirred with the solution for one hour. The THF is evaporated and the water is extracted with chloroform. Drying over magnesium sulfate and evaporation of the chloroform gives a yellow oil. Flash chromatography in ethyl acetate on silica gel gives 1.5 g (65%) of 1-(4'-hydroxy,3'-methoxyphenyl)-4-phenoxy-1-butene-3-one; mp=85°-87° C. C, H analysis Calcd for C17H16O4 (71.81, 5.68); Found (71.85, 5.50).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04959503 |
|---|
| Source dataset | uspto-grants-1990_09 |
|---|
| ORD ID | ord-5356df36477b4f1989f774563696b752 |
|---|
| Source note | uspto-grants-1990_09 |
|---|