HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019261Generated: October 29, 2026
EDTA disodium salt → 1,1-Dioxo-tetrahydro-thiopyran-4-one
https://huagongshe.com/reaction/1019261
Participants
| Role | Name | HCID | Charge |
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| Reactant | EDTA disodium salt | HCID 8759 | — |
| Reactant | Tetrahydrothiopyran-4-one | HCID 66173 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,1-Dioxo-tetrahydro-thiopyran-4-one | HCID 262230 | 73% |
Reaction Steps
To a solution of tetrahydrothiopyran-4-one (400 mg, 3.45 mmol) in acetonitrile (5 ml) was added aqueous Na2EDTA (3 ml, 0.0004 M). A mixture of oxone (6.30 g, 10.30 mmol) and sodium bicarbonate (2.70, 32 mmol) was added in small portions to the above solution over a period of 20 min. The slurry was stirred for another 1 h before being quenched with methylene chloride. The organic solvent was decanted and the solid residue was triturated with ethyl acetate (3×25 ml). The combined organic layers were dried over sodium sulfate and concentrated to give the desired ketone (0.37 g, 73%) as a colorless solid. mp 170-172° C. (lit. 168-170° C.); 1H NMR (500 MHz, CDCl3) 2.99 (t, J=6.8 Hz, 4H), 3.39 (t, J=6.8 Hz, 4H). Ref: Yang, D.; Yip, Y.-C.; Jiao, G.-S.; Wong, M.-K. Design of Efficient Ketone Catalysts for Epoxidation by Using the Field Effect. J. Org. Chem, 1998, 63, 8952-8956.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06486199B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-5f4e95a0a41845d28606c847560c838c |
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| Source note | uspto-grants-2002_11 |
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