HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64703Erstellt: 26. Oktober 2026
N,N-Dimethylaniline → 16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-one
https://huagongshe.com/reaction/64703
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N-Dimethylaniline | HCID 949 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Bromoacetyl bromide | HCID 61147 | — |
| Edukt | Oxendolone | HCID 443947 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-one | HCID 15593764 | 74,6% |
Reaktionsschritte
In 40 ml of dichloromethane are dissolved 4.5 g of 16β-ethyl-17β-hydroxy-4-estren-3-one and 1.8 g of N,N-dimethylaniline and, with ice-cooling and stirring, a solution of 3.5 g of bromoacetyl bromide in 5 ml of dichloromethane is added dropwise to the above solution. The mixture is stirred with ice-cooling for 30 minutes and at room temperature (15°-25° C.) for 5 hours, and 200 ml of ethyl acetate is added. The mixture is washed with 10% cold sulfuric acid (three times), water and saturated aqueous sodium chloride solution in that order and dried over anhydrous sodium sulfate. The solvent is then distilled off under reduced pressure. The residue is recrystallized from diisopropyl ether-petroleum ether (1:1) to give 4.7 g of the above-identified compound as colorless crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04609650 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-18bde555835b47f78c6ab8bfa5bd8bba |
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| Quellennotiz | uspto-grants-1986_09 |
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