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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276565Erstellt: 24. Oktober 2026

Ethanolamine → 1-Aminocyclopentanemethanol

https://huagongshe.com/de/reaction/276565

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
Edukt4-Nitro-m-toluidineHCID 11898—
EduktThionyl ChlorideHCID 24386—
Edukt3-Methyl-4-nitrophenyl isothiocyanateHCID 18316341—
Produkt1-AminocyclopentanemethanolHCID 66307—
Produkt1-(Chloromethyl)cyclopentan-1-amine hydrochlorideHCID 69992485—

Reaktionsschritte

3-Methyl-4-nitroaniline was converted to 3-methyl-4-nitrophenyl isothiocyanate according to Method A2a, Step 3. 1-Amino-1-(hydroxymethyl)cyclopentane was synthesized as described in Method B1c. The 2-hydroxyethylamine was reacted with SOCl2 according to Method B7a to give 1-amino-1-(chloromethyl)cyclopentane HCl salt. The 2-chloroethylamine was reacted with 3-methyl-4-nitrophenyl isothiocyanate according to Method C1a to give 2-(3-methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonane. The thiazolidine was reacted with isobutyl bromide according to Method D2a to afford 1-isobutyl-2-(3-methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-17d5ace8ff2d483185d1251b3dd072d2
Quellennotizuspto-grants-2002_03