HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1413132Erstellt: 26. Oktober 2026
Triethylamine → N-[1-(benzyl)-2-(phenyl)-ethyl]-cis-2-Octyl-cyclopropanoctanamide
https://huagongshe.com/reaction/1413132
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | 1,3-Diphenyl-2-aminopropane | HCID 77960 | — |
| Edukt | cis-8-(2-Octylcyclopropyl) octanoic acid | HCID 11426463 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-[1-(benzyl)-2-(phenyl)-ethyl]-cis-2-Octyl-cyclopropanoctanamide | HCID 13131904 | — |
Reaktionsschritte
To a cooled solution of 2.0 g (cis)-2-octylcyclopropanoctanoic acid in 70 ml methylene chloride at -20° is added first 0.707 g triethylamine and then dropwise 0.732 g ethylchloroformate. The reaction mixture is then allowed to come to room temperature and stirred for 1 hours. Then 1.5 g of 1-benzyl-2-(phenyl)ethylamine is added, and the reaction mixture stirred for 16 hours. The reaction mixture is then extracted a few times with 2 N hydrochloric acid, then with 2 N aq. sodium hydroxide sol. and washed several times with saturated aq. sodium chloride. The organic phase is then dried over anh. sodium sulphate filtered and evaporated i.v. to dryness to obtain a residue, which upon crystallization from pentane yields the title product (m.p. 40°-45°).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04248893 |
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| Quelldatensatz | uspto-grants-1981_02 |
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| ORD ID | ord-b3e450c85cb64983be9d4080d00244ec |
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| Quellennotiz | uspto-grants-1981_02 |
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