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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276487Erstellt: 24. Oktober 2026

Ethanolamine → 4-Amino-3-methylbenzonitrile

https://huagongshe.com/de/reaction/276487

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktAnilineHCID 6115—
EduktL-Isoleucine, methyl esterHCID 75735—
Edukt(2S)-2-amino-3-methylpentan-1-olHCID 11789185—
Edukt4-Cyano-2-methylphenyl isothiocyanateHCID 18316299—
Produkt4-Amino-3-methylbenzonitrileHCID 7010316—
ProduktHCID 178445843HCID 178445843—

Reaktionsschritte

(1S)-1-(Hydroxymethyl)-2-methylbutylamine was made from (L)-isoleucine methyl ester as described in Method B1b. The 2-hydroxyethylamine was converted to (1S)-1-(chloromethyl)-2-methylbutanammonium chloride as described in Method B7a. 4-Cyano-2-methylaniline was synthesized as described in Method A1a. The aniline was converted to 4-cyano-2-methylphenyl isothiocyanate as described in Method A2a, Step 3. 4-Cyano-2-methylphenyl isothiocyanate was reacted with (1S)-1-(chloromethyl)-2-methylbutanammonium chloride to Method C1a to give (4S)-2-(4-cyano-2-methylphenylimino)-4-(2-butyl)-1,3-thiazolidine. The thiazolidine was reacted with isobutyl bromide according to Method D2a to give (4S)-2-(4-cyano-2-methylphenylimino)-4-butyl-3-isobutyl-1,3-thiazolidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-f2ed8f833b1442dc8ea4d3b91a740237
Quellennotizuspto-grants-2002_03