HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66400Erstellt: 24. Oktober 2026
Acetic Acid → trans-4-[2-(Dimethylamino)-ethyl]-4-cyclohexene-1,2-diol
https://huagongshe.com/de/reaction/66400
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Iodine | HCID 807 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 1-[2-(Dimethylamino)ethyl]-1,4-cyclohexadiene | HCID 12228920 | — |
| Katalysator | Silver acetate | HCID 11246 | — |
| Produkt | trans-4-[2-(Dimethylamino)-ethyl]-4-cyclohexene-1,2-diol | HCID 54092690 | — |
Reaktionsschritte
A solution of 45 g. (0.3 moles) of 1-[2-(dimethylamino)-ethyl]-1,4-cyclohexadiene from Example 3(a) in 1.5 l. of dry glacial acetic acid is treated with 100 g. of silver acetate and 75 g. of iodine. The mixture is stirred until most of the iodine dissolves and is then heated for two hours at 95°. The reaction solution is cooled, filtered and evaporated in vacuo to give an oil. The oil is taken up in ethyl acetate and washed with aqueous sodium bicarbonate solution. The organic phase is dried (MgSO4) and evaporated to an oil. The oil is taken up in ethyl acetate and treated with HCl in isopropanol. The resulting crude solid is removed by filtration and recrystallized from acetonitrile-ether to yield dl-trans-4-[2-(dimethylamino)-ethyl]-4-cyclohexene-1,2-diol, diacetate ester, hydrochloride salt.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04131744 |
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| Quelldatensatz | uspto-grants-1978_12 |
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| ORD ID | ord-b120cb378f7d474b876bc775b36ea058 |
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| Quellennotiz | uspto-grants-1978_12 |
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