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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717253Generated: November 4, 2026

Ethyl 3-oxohexanoate → HCID 68517172, compound

https://huagongshe.com/reaction/1717253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-oxohexanoateHCID 238498—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 86629793HCID 86629793—
SolventEthanolHCID 702—
ProductHCID 68517172HCID 68517172100%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-azido-N-(2,2,2-trifluoroethyl)benzamide (0.98 g) obtained in Example 46a) and ethyl 3-keto-n-hexanoate (0.77 ml) in ethanol (20 ml) was added 20% sodium ethoxide in ethanol solution (1.85 ml) at room temperature, and the mixture was stirred overnight at 60° C. The reaction mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure. The residue was diluted with water, and washed with ethyl acetate. The aqueous layer was acidified with 1N hydrochloric acid, and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound as a pale-brown amorphous solid (1.4 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803822B2
Source datasetuspto-grants-2010_09
ORD IDord-aa34a321e21540fc8b9ac9b9f68923fb
Source noteuspto-grants-2010_09