HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Methyl-4-nitrophenyl isothiocyanate → 2-(2-Methyl-4-nitrophenylimino)-3-(cyclopentylmethyl)-1,3-thiazolidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Methyl-4-nitrophenyl isothiocyanate | HCID 145621 | — |
| Edukt | N-cyclopentylmethyl-N-(2-chloroethyl)ammonium chloride | HCID 18316280 | — |
| Produkt | 2-(2-Methyl-4-nitrophenylimino)-3-(cyclopentylmethyl)-1,3-thiazolidine | HCID 18316192 | — |
Reaktionsschritte
2-Hydroxyethylamine was reacted with cyclopentylmethyl bromide according to Method B2a to give N-cyclopentylmethyl-N-(2-hydroxyethyl)amine. The alcohol was reacted with SOCl2 according to Method B7c to give N-cyclopentylmethyl-N-(2-chloroethyl)ammonium chloride. The chloroethylamine was reacted with 2-methyl-4-nitrophenyl isothiocyanate to give 2-(2-methyl-4-nitrophenylimino)-3-(cyclopentylmethyl)-1,3-thiazolidine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06353006B1 |
| Quelldatensatz | uspto-grants-2002_03 |
| ORD ID | ord-27f621abef0947c88fc46b7e03ab51ca |
| Quellennotiz | uspto-grants-2002_03 |