HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6459Erstellt: 23. Oktober 2026
Water → (4R-cis)-1,1-dimethylethyl 6-(4-chlorobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetate
https://huagongshe.com/de/reaction/6459
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate | HCID 9816650 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (4R-cis)-1,1-dimethylethyl 6-(4-chlorobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetate | HCID 11797121 | 130,1% |
Reaktionsschritte
To a stirring, 0°-5° C. solution of the (4R-cis)-1,1-dimethylethyl 6-hydroxymethyl-2,2-dimethyl-1,3-dioxane-4-acetate (European Patent Application 0319,847) (10 g, 38 mmol) in methylene chloride (250 mL) containing triethylamine (10 mL, 72 mmol) is added 4-chlorobenzenesulfonyl chloride (12.7 g, 60 mmol). Stirring is continued at 0°-5° C. for 2.5 hours and the solution slowly warmed to 20°-25° C. over a period of 2 hours. The solution is poured onto 200 mL of water and the layers separated. The upper aqueous layer is extracted with 200 mL of methylene chloride and the combined organic layers are washed with 200 mL each of saturated sodium bicarbonate solution to ensure complete removal of 4-chlorobenzenesulfonyl chloride and then saturated sodium chloride solution. Drying the solution with magnesium sulfate and concentration in vacuo gives 21.5 g of the product as a pale yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05248793 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-25c2d201df154c4a8596ac428de335f8 |
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| Quellennotiz | uspto-grants-1993_09 |
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