HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 848895Erstellt: 25. Oktober 2026
Propargyl bromide → 7-Chloro-4-hydroxy-4-methyl-1-heptyne
https://huagongshe.com/reaction/848895
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Propargyl bromide | HCID 7842 | — |
| Edukt | 1,1-Dibromoethane | HCID 11201 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 2-Pentanone, 5-chloro- | HCID 79993 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 7-Chloro-4-hydroxy-4-methyl-1-heptyne | HCID 12898739 | — |
Reaktionsschritte
To a mixture of 6.69 g. of magnesium in 20 ml. of ether under argon, is added 0.1 g. of mercuric chloride and 0.1 g. of dibromoethane. The mixture is stirred for 10 minutes and 0.5 ml. of propargyl bromide is added. A 50 ml. portion of ether is added, followed by a solution of 30 g. of 5-chloro-2-pentanone and 32.55 g. of propargyl bromide in 45 ml. of ether with stirring, at a rate to maintain vigorous reflux. The mixture is stirred an additional 15 minutes, cooled to -5° C. and an ice cold saturated solution of ammonium chloride is added dropwise. The ether layer is decanted and filtered. The solids are washed with ether which is also filtered. The combined ether filtrates are washed with water, dried over magnesium sulfate and the solvent removed giving the product as an orange oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04297516 |
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| Quelldatensatz | uspto-grants-1981_10 |
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| ORD ID | ord-de835914cdc24d37b15db793170575e7 |
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| Quellennotiz | uspto-grants-1981_10 |
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