HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Methyl indane-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Mercapto-Indan-2-Carboxylic Acid Methyl Ester | HCID 20766012 | — |
| Reactant | Chloride 5-chloromethyl-4-methyl-2-(4-trifluoromethyl-phenyl)-thiazole | HCID 21949469 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl indane-2-carboxylate | HCID 9964238 | 68.4% |
Reaction Steps
Compound 1C (crude mixture from above, 830 mg) was dissolved in acetonitrile (80 mL) with the chloride 5-chloromethyl-4-methyl-2-(4-trifluoromethyl-phenyl)-thiazole (0.50 g, 1.71 mmol) and Cs2CO3 (2.37 g, 7.27 mmol) The reaction mixture was stirred at RT overnight. Ether (50 mL) and H2O were added and stirring was continued for another 5 min. The layers were separated and the aqueous layer was extracted with ether (2×100 mL). The combined organics was dried over MgSO4 and concentrated to an oil. The crude product was purified by column chromatography eluted with EtOAc and hexanes to give the desired product as a thick yellow oil (0.48 g, 28% for 2 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06867224B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-b11fc74cb8e4429d986ab6c78c31ff56 |
| Source note | uspto-grants-2005_03 |