HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479243Generated: October 29, 2026
(Benzyloxycarbonyl-ethoxy-methyl)-triphenyl-phosphonium chloride → [Rac]-2-ethoxy-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-3-propyl-phenyl}-propionic acid
https://huagongshe.com/reaction/479243
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Benzyloxycarbonyl-ethoxy-methyl)-triphenyl-phosphonium chloride | HCID 18003460 | — |
| Reactant | (Benzyloxycarbonyl-methoxy-methyl)-triphenyl-phosphonium chloride | HCID 18003490 | — |
| Reactant | 3-Allyl-4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-benzaldehyde | HCID 18003531 | — |
| Product | [Rac]-2-ethoxy-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-3-propyl-phenyl}-propionic acid | HCID 18003555 | — |
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 |
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| Patent number | US06642389B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-0fd367147df44592a335b73939480185 |
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| Source note | uspto-grants-2003_11 |
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