HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751952Generated: October 28, 2026
HCID 86646120, compound → HCID 86646121, compound
https://huagongshe.com/reaction/1751952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86646120 | HCID 86646120 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 86646121 | HCID 86646121 | — |
Reaction Steps
Ethyl 4-ethyl-3-hydroxyhept-6-enoate (3.64 g, 18.2 mmol) was dissolved in a 2 N solution of potassium hydroxide in methanol (120 mL), and the solution was stirred overnight at room temperature. From the reaction solution, the solvent was distilled off under reduced pressure. To the residue, a 1 N aqueous sodium hydroxide solution (200 mL) was then added, followed by extraction with diethyl ether. The aqueous layer was made acidic by the addition of concentrated hydrochloric acid under ice cooling, followed by extraction with diethyl ether again. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain the compound of interest as a pale yellow oil substance (3.14 g, <100%, mixture of diastereomers).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09162971B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-9b3879a819a841cfb4a0270d9f55d5eb |
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| Source note | uspto-grants-2015_10 |
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