HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717253Generated: November 4, 2026
Ethyl 3-oxohexanoate → HCID 68517172, compound
https://huagongshe.com/reaction/1717253
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-oxohexanoate | HCID 238498 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 86629793 | HCID 86629793 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68517172 | HCID 68517172 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803822B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-aa34a321e21540fc8b9ac9b9f68923fb |
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| Source note | uspto-grants-2010_09 |
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