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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500139Generated: November 4, 2026

HCID 86646120, compound → HCID 86646121, compound

https://huagongshe.com/reaction/1500139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86646120HCID 86646120—
SolventMethanolHCID 887—
SolventPotassium HydroxideHCID 14797—
ProductHCID 86646121HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206104B2
Source datasetuspto-grants-2015_12
ORD IDord-ad9de9f52f09460ba00e0b98976dc1b6
Source noteuspto-grants-2015_12