HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzene → 2-(2,3,5,6-Tetramethylbenzyl)aminoheptane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzene | HCID 241 | — |
| Edukt | 2-Aminoheptane | HCID 5603 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3-(Chloromethyl)-1,2,4,5-tetramethylbenzene | HCID 81939 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2-(2,3,5,6-Tetramethylbenzyl)aminoheptane | HCID 20553695 | — |
Reaktionsschritte
36.5 g (0.2 mol) of 2,3,5,6-tetramethylbenzyl chloride, 46.0 g (0.4 mol) of 2-aminoheptane and 100 ml of benzene are refluxed for 2 hours. The solvent is then removed in vacuo. A solution of 8 g (0.2 mol) of sodium hydroxide in methanol is then added to the residue to liberate the free base. The reaction product is separated from the precipitated sodium chloride by means of a suction filter, and the excess of 2-aminoheptane is removed by vacuum distillation. The 2-(2,3,5,6-tetramethylbenzyl)aminoheptane obtained is then treated with ethereal hydrochloric acid to convert it into the hydrochloride which is recrystallised from methanol/ethyl acetate. The melting point of the hydrochloride is 155° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04312861 |
| Quelldatensatz | uspto-grants-1982_01 |
| ORD ID | ord-9389f15663104cc3b8a3af975bde95be |
| Quellennotiz | uspto-grants-1982_01 |