HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199589Generated: October 26, 2026
Acetic Acid → ethyl 3-oxotetrahydro-2H-thiopyran-2-carboxylate
https://huagongshe.com/reaction/2199589
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl 4-[(2-ethoxy-2-oxoethyl)thio]butanoate | HCID 2778847 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | ethyl 3-oxotetrahydro-2H-thiopyran-2-carboxylate | HCID 12269128 | 34.2% |
Reaction Steps
To a solution of 5 g (219 mmol) of sodium in 13 mL of anhydrous EtOH and 88 mL of ether are added dropwise, at 0° C. and under argon, 20.5 g (87.5 mmol) of ethyl 4-[(2-ethoxy-2-oxoethyl)sulfanyl]butanoate. After stirring for 18 hours at room temperature, the reaction mixture is poured into a mixture of AcOH (12 mL)/ice (70 g). The medium is then concentrated under reduced pressure, and the residue obtained is taken up in 100 mL of ether, washed with brine (2×50 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue obtained is purified by chromatography on silica gel, eluting with a cyclohexane/EtOAc gradient of from 0 to 10% EtOAc. 5.64 g of ethyl 3-oxotetrahydro-2H-thiopyrane-2-carboxylate are obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359329B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-f76f5020d8da4ff987eb733623ef7ec0 |
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| Source note | uspto-grants-2016_06 |
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