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HRID 743421Erstellt: 25. Oktober 2026
2,6-Dichlorobenzoic acid → 2-(2,6-Dichlorophenylcarbonyloxymethyl)-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide
https://huagongshe.com/reaction/743421
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2,6-Dichlorobenzoic acid | HCID 5758 | — |
| Edukt | Thallium | HCID 5359464 | — |
| Edukt | 2-Chloromethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide | HCID 19424425 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(2,6-Dichlorophenylcarbonyloxymethyl)-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide | HCID 15838069 | 29% |
Reaktionsschritte
The thallium salt of 2,6-dichlorobenzoic acid (0.96 g; 2.43 mmol, prepared from 0.46 g of 2,6-dichlorobenzoic acid and 0.605 g of TlOC2H5 in ethanol ) was added to a solution of 2-chloromethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (0.5 g; 2.21 mmol) in DMF (10 ml) containing tetrabutylammonium bromide (70 mg; 0.22 mmol). The mixture was allowed to react at 50° C. for 15 hours and at 100° C. for an additional hour, and then cooled. The mixture was concentrated in vacuo and the residue was purified by flash chromatography (25%-30% ethyl acetate in hexane) to afford 0.24 g (29%) of 2-(2,6-dichlorophenylcarbonyloxymethyl)-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (Formula I: Ar=2,6-Cl2 -phenyl; R1 =H; R2 =propyl; R3 =H) as a solid, m.p.95°-97° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05556909 |
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| Quelldatensatz | uspto-grants-1996_09 |
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| ORD ID | ord-43730bc26c034a619390e78ce92ec417 |
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| Quellennotiz | uspto-grants-1996_09 |
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