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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717335Generated: November 5, 2026

Ethyl 3-oxohexanoate → HCID 68518077, compound

https://huagongshe.com/reaction/1717335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-oxohexanoateHCID 238498—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 86629806HCID 86629806—
SolventEthanolHCID 702—
ProductHCID 68518077HCID 6851807757%

Reaction Steps

To a solution of 6-azido-3,4-dihydroisoquinolin-1(2H)-one (0.24 g) obtained in Example 132b) and ethyl 3-keto-n-hexanoate (0.25 ml) in ethanol (7 ml) was added 28% sodium ethoxide in ethanol solution (0.60 ml) at room temperature, and the mixture was stirred for 3 hr. The solvent was evaporated under reduced pressure, and water was added to the obtained residue. The mixture was washed with ethyl acetate, 1N hydrochloric acid was added to acidify the aqueous solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound as a yellow solid (0.22 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803822B2
Source datasetuspto-grants-2010_09
ORD IDord-72d9041d3be9446e9ba27aaedde1e8f1
Source noteuspto-grants-2010_09