HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479242Generated: November 1, 2026
3-Allyl-4-hydroxybenzaldehyde → 3-Allyl-4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-benzaldehyde
https://huagongshe.com/reaction/479242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Allyl-4-hydroxybenzaldehyde | HCID 4729014 | — |
| Reactant | 2-(5-Methyl-2-phenyl-1,3-oxazol-4-yl)ethyl methanesulfonate | HCID 10540773 | — |
| Product | 3-Allyl-4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-benzaldehyde | HCID 18003531 | — |
Reaction Steps
In analogy to the procedures described in examples 114 b], c] and d], 3-allyl-4-hydroxy-benzaldehyde was reacted with methanesulfonic acid 2-(5-methyl-2-phenyl-oxazol-4-yl)-ethyl ester [PCT Int. Appl. (2000) WO0008002] to give 3-allyl-4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-benzaldehyde. Treatment of 3-allyl-4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-benzaldehyde with (benzyloxycarbonyl-ethoxy-methyl)-triphenyl-phosphonium chloride (prepared in analogy to the procedure described for the synthesis of (benzyloxycarbonyl-methoxy-methyl)-triphenyl-phosphonium chloride in example 114 a]) then gave 3-{3-allyl-4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-phenyl}-2(Z,E)-ethoxy-acrylic acid benzyl ester, which was hydrogenated to yield [rac]-2-ethoxy-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-3-propyl-phenyl}-propionic acid as colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06642389B2 |
|---|
| Source dataset | uspto-grants-2003_11 |
|---|
| ORD ID | ord-d8d8469790ce445a986f1b3ecc8be067 |
|---|
| Source note | uspto-grants-2003_11 |
|---|