HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112725Erstellt: 25. Oktober 2026
Chloroacetyl chloride → N-(4-chlorophenacyl) chloroacetamide
https://huagongshe.com/reaction/1112725
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloroacetyl chloride | HCID 6577 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochloride | HCID 2798211 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(4-chlorophenacyl) chloroacetamide | HCID 53685377 | 57,3% |
Reaktionsschritte
To a well stirred suspension of 20.6 g of 4-chlorophenacylamine hydrochloride in 70 ml of benzene and 70 ml of water which was cooled to below 7° C. were added simultaneously 110 ml of 2N NaOH solution and 12.4 g of chloroacetyl chloride dissolved in 30 ml of benzene. After the addition was complete, the reaction mixture was warmed to room temperature and stirred at room temperature for 3 hours. At the end of this period, the formed precipitate was filtered, and the benzene layer was separated. The aqueous layer was extracted twice with 50 ml of benzene. The combined benzene layer was dried over anhydrous sodium sulfate, and evaporated to dryness. The residue together with the precipitate obtained above was combined and recrystallized from ethanol to give 14.1 g (57 percent) of N-(4-chlorophenacyl) chloroacetamide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04123541 |
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| Quelldatensatz | uspto-grants-1978_10 |
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| ORD ID | ord-6bcbf79b75444c858797bc73afb2fc3e |
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| Quellennotiz | uspto-grants-1978_10 |
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