HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420404Generated: October 25, 2026
Potassium Carbonate → HCID 57586498, compound
https://huagongshe.com/reaction/420404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57586512 | HCID 57586512 | — |
| Reactant | HCID 178502985 | HCID 178502985 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57586498 | HCID 57586498 | 71.3% |
Reaction Steps
To a 0° C. solution of 4-[2-(2-Ethoxycarbonyl-ethyl)-3-(6-oxo-hexyl)-phenoxy]-butyric acid ethyl ester (7.0 g, 17.24 mmol) and potassium carbonate (7.14 g, 51.72 mmol) in MeOH (200 mL), the Ohira's reagent (ref. cited in Synlett, 1996, 521) (6.3 g, 32.8 mmol) in MeOH (50 mL) was added slowly. The cooling bath was removed upon the end of addition and the reaction mixture stirred at room temperature for 5 hr. The reaction was then extracted with EtOAc and brine. The combined organic layers were dried over sodium sulfate then evaporated under vacuo. The crude material was purified by column chromatography using 50% EtOAc-Hexane as eluant to give the title compound (4.6 g, 71%) as a light yellow oil. HR-ES(+): calculated for C22H30O5 (M+Na)1+ 397.1985, found 397.1985.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093385B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c283fb61c69a4aafb6146e4644833d3c |
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| Source note | uspto-grants-2012_01 |
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