HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670152Generated: October 26, 2026
Potassium Carbonate → HCID 57586498, compound
https://huagongshe.com/reaction/1670152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[2-(2-Ethoxycarbonyl-ethyl)-3-(6-oxo-hexyl)-phenoxy]-butyric acid ethyl ester | HCID 57586512 | — |
| Reactant | HCID 178502985 | HCID 178502985 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57586498 | HCID 57586498 | 71.3% |
Reaction Steps
To a solution of 4-[2-(2-ethoxycarbonyl-ethyl)-3-(6-oxo-hexyl)-phenoxy]-butyric acid ethyl ester (7.0 g, 17.24 mmol) was added a solution of potassium carbonate (7.14 g, 51.72 mmol) in MeOH (200 mL) and the resulting mixture was cooled to 0° C. Then 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 was stirred at room temperature for 5 hr. The reaction was then extracted into ethyl acetate and washed with brine. The combined organic extracts were dried over sodium sulfate and concentrated under reduced pressure. The crude material was purified by column chromatography using 50% ethyl acetate-hexanes as eluant to give the title compound (4.6 g, 71%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989454B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-ea39efaec0b74ec1a70f4149655b5af8 |
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| Source note | uspto-grants-2011_08 |
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