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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1905823Erstellt: 27. Oktober 2026

Hydrochloric Acid → 2-Amino-6-(4-aminophenyl)-6-methylheptane

https://huagongshe.com/reaction/1905823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAnilineHCID 6115—
EduktHeptaminol HydrochlorideHCID 10969—
EduktSodium HydroxideHCID 14798—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelWaterHCID 962—
Produkt2-Amino-6-(4-aminophenyl)-6-methylheptaneHCID 2015666982%

Reaktionsschritte

To a solution of 34 parts of anhydrous zinc chloride in 51 parts of 36& w/w aqueous hydrochloric acid were added 46.5 parts of aniline and 18.2 parts of 6-hydroxy-6-methyl-2-heptylamine hydrochloride. The whole was charged to a 3-necked round bottomed flask fitted with a thermometer, stirrer, and Dean and Stark water separator. The stirred reaction mixture heated by means of an electric heating mantle was raised to a temperature of 185° C. by removal of water (Dean and Stark), and then maintained at this temperature for a further 18 hours. The hot reaction mixture was then poured slowly into a solution of 75 parts sodium hydroxide in 75 parts water and stirred until cool. The organic phase was extracted with ether, washed with water, evaporated and distilled under reduced pressure. After recovering 28 parts of aniline, there was obtained 18 parts of 2-amino-6-(4-aminophenyl)-6-methylheptane b12 192°-199° C. (82% yield based on heptaminol) with the following percentage composition by weight.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04647699
Quelldatensatzuspto-grants-1987_03
ORD IDord-e0128aba3d9e43c8afd1451ba2df2749
Quellennotizuspto-grants-1987_03