HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1376833Erstellt: 25. Oktober 2026
Diethyl Ether → 1,1-Dimethylethyl 2-chloro-3-(4-chlorophenyl)-oxirane carboxylate
https://huagongshe.com/reaction/1376833
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Edukt | 1,1-Dimethylethyl dichloroacetate | HCID 3016483 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1,1-Dimethylethyl 2-chloro-3-(4-chlorophenyl)-oxirane carboxylate | HCID 22916901 | 21,9% |
Reaktionsschritte
5.55 g of tert.-butyl dichloroacetate in 30 ml of tetrahydrofuran were stirred while 4.64 g of 4-chlorobenzaldehyde were added, and after cooling to -20° C., 30 ml of an N solution of potassium tert.-butylate in tetrahydrofuran were added. The temperature was allowed to rise to 20° C. and after 20 minutes, 50 ml of ether and 40 ml of water saturated with sodium chloride were added, with stirring for 5 minutes. The decanted organic phase was washed with water saturated with sodium chloride, then dried and concentrated to dryness under reduced pressure. The residue was chromatographed on silica and eluted with methylene chloride to obtain 1.90 g of 1,1-dimethylethyl 2-chloro-3-(4-chlorophenyl)-oxirane carboxylate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05663164 |
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| Quelldatensatz | uspto-grants-1997_09 |
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| ORD ID | ord-e732cd25f67246d498489bc149eae694 |
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| Quellennotiz | uspto-grants-1997_09 |
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