HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Aminoheptane → 1-sec-heptyl-3-n-hexyl-2-S-ethylisothiourea
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Aminoheptane | HCID 5603 | — |
| Edukt | Iodoethane | HCID 6340 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Hexyl isothiocyanate | HCID 78120 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-sec-heptyl-3-n-hexyl-2-S-ethylisothiourea | HCID 13083466 | — |
Reaktionsschritte
The equipment, procedure and reactants were the same as in Example 31 with the exception that 10.01 g (0.07 mole) of n-hexylisothiocyanate, 8.05 g (0.07 mole) 2-aminoheptane, 35 ml ethanol 2B, 11.7 g (0.075 mole) ethyl iodide, 200 ml of toluene and a one percent solution sodium hydroxide (0.08 mole) were used as reactants and reagents in the procedure. The reaction produced 19.6 g (98 weight percent of theory yield of a clear liquid having a nD30 of 1.4765. The product was identified as the title product by IR and NMR spectra analyses.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04515813 |
| Quelldatensatz | uspto-grants-1985_05 |
| ORD ID | ord-eb18b9da3bd24229821e66ed16e08c60 |
| Quellennotiz | uspto-grants-1985_05 |