Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276487Generated: October 25, 2026

Ethanolamine → 4-Amino-3-methylbenzonitrile

https://huagongshe.com/reaction/276487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantAnilineHCID 6115—
ReactantL-Isoleucine, methyl esterHCID 75735—
Reactant(2S)-2-amino-3-methylpentan-1-olHCID 11789185—
Reactant4-Cyano-2-methylphenyl isothiocyanateHCID 18316299—
Product4-Amino-3-methylbenzonitrileHCID 7010316—
ProductHCID 178445843HCID 178445843—

Reaction Steps

(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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-f2ed8f833b1442dc8ea4d3b91a740237
Source noteuspto-grants-2002_03