HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393394Generated: November 3, 2026
Potassium Carbonate → 2-Methyl-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-phenyl}-2-m-tolyloxy-propionic Acid
https://huagongshe.com/reaction/1393394
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(5-Methyl-2-phenyloxazol-4-yl)ethyl 4-methylbenzenesulfonate | HCID 12051739 | — |
| Reactant | 3-(4-Hydroxyphenyl)-2-methyl-2-m-tolyloxy-propionic acid ethyl ester | HCID 69316184 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methyl-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-phenyl}-2-m-tolyloxy-propionic Acid | HCID 22339962 | — |
Reaction Steps
Standard Procedure (B): A mixture of 3-(4-hydroxy-phenyl)-2-methyl-2-m-tolyloxy-propionic acid ethyl ester (0.095 g, 0.030 mmol), toluene-4-sulfonic acid 2-(5-methyl-2-phenyl-oxazol-4-yl)-ethyl ester (0.108 g, 0.030 mmol) and 325 mesh K2CO3 (0.084 g, 0.60 mmol) in ethanol (2 mL) was heated to reflux for 24 h under N2. Aqueous 5N NaOH (0.5 mL) and additional ethanol (1 mL) was added to the reaction mixture and it was heated at reflux for an additional 2 h. The reaction was cooled and the solvent removed in vacuo. The residue was acidified with aqueous 1 N HCl (5 mL), extracted with water and CH2Cl2 and the organic layer dried by passing it through a Varian Chem Elut 1003 cartridge. The solvent was removed in vacuo to give 0.134 g of crude product which was purified by LCMS to give 0.036 g (25%) of analytically pure 2-methyl-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-phenyl}-2-m-tolyloxy-propionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07345070B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-3cf92d2e72d54ddeb4571d22740abf04 |
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| Source note | uspto-grants-2008_03 |
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