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HRID 2255254Erstellt: 24. Oktober 2026
Ethanol → (2,6-Diisopropyl-phenylsulfamoyl)-acetic acid ethyl ester
https://huagongshe.com/de/reaction/2255254
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | Sulfoacetic acid | HCID 31257 | — |
| Edukt | Diisopropylaniline | HCID 32484 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (2,6-Diisopropyl-phenylsulfamoyl)-acetic acid ethyl ester | HCID 44330987 | — |
Reaktionsschritte
Sulfoacetic acid (52 g, 371 mM) and EtOH (500 mL) were heated under reflux for 20 hours. The reaction mixture was cooled, and the excess ethanol was removed under vacuum to give 2 (see Chart I). A mixture of 2 (16.82 g, 100 mM) and POCl3 (30.67 g, 200 mM) was heated at 125° C. for 5 hours. The mixture was cooled and filtered, and excess POCl3 was removed to give 3 (see Chart I). Compound 3 (8.18 g, 43.83 mM) was added dropwise with stirring to a solution of 2,6-diisopropylaniline (15.54 g, 87.66 mM) in 50 mL CH2Cl2 maintained at 0° C. The mixture was stirred at room temperature for an additional 18 hours. The solvent was removed and the residue was redissolved in 100 mL ethyl acetate and washed with 1 N HCl and brine. The ethyl acetate was evaporated and the pure compound was isolated by chromatography over silica gel (EtOAc/hexane, 1:4 as eluant) as a white powder, 7.0 g (~50%), mp 114°-116° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05239082 |
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| Quelldatensatz | uspto-grants-1993_08 |
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| ORD ID | ord-f50c8b709851438080f600e477ebcc2b |
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| Quellennotiz | uspto-grants-1993_08 |
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