HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 224331Erstellt: 24. Oktober 2026
Triethylamine → Benzeneacetamide, N-(2-(2,3-dihydro-6-methyl-1H-inden-5-yl)ethyl)-3,4-dimethoxy-
https://huagongshe.com/de/reaction/224331
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | (3,4-Dimethoxyphenyl)acetyl chloride | HCID 3604458 | — |
| Edukt | 5-Aminoethyl-6-methylindan | HCID 12426124 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | Benzeneacetamide, N-(2-(2,3-dihydro-6-methyl-1H-inden-5-yl)ethyl)-3,4-dimethoxy- | HCID 3051196 | — |
Reaktionsschritte
5-Aminoethyl-6-methylindan (4.0 g, 0.029 mole) was dissolved in 100 ml of dry benzene, 4 ml of triethylamine was added and a solution of the previously prepared 3,4-dimethoxyphenylacetyl chloride in dry benzene was added to the substituted indan mixture. The reaction mixture was refluxed for several hours and then gently heated overnight at a temperature below reflux. The reaction was then cooled, washed with 3×100 ml of 20% HCl solution, 3×100 ml of 8% NaHCO3 solution and 2×125 ml of water. The benzene layer was then reduced in volume on a rotary evaporator to yield a solid precipitate. The solid was filtered, washed with benzene, air dried to yield a slightly pink powder (3.5 g, mp 144°-145° C.). The crude product was then recrystallized from benzene (large volume), mp 144°-144.5° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04232014 |
|---|
| Quelldatensatz | uspto-grants-1980_11 |
|---|
| ORD ID | ord-663cc495f71a4c84924194f9d7641ca3 |
|---|
| Quellennotiz | uspto-grants-1980_11 |
|---|