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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21361Erstellt: 25. Oktober 2026

Acetic Acid → N-(4'-iodophenyl)-2-aminooctane

https://huagongshe.com/reaction/21361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1,1-DichloroethaneHCID 6365—
Edukt2-OctanoneHCID 8093—
Edukt4-IodoanilineHCID 10893—
EduktSodium triacetoxyborohydrideHCID 5049666—
ProduktN-(4'-iodophenyl)-2-aminooctaneHCID 992752188,2%

Reaktionsschritte

A flask containing 4-iodoaniline (11.0 g, 50.2 mmol) was charged with dry dichloroethane (125 ml), 2-octanone (7.9 ml, 50.0 mmol) and sodium triacetoxyborohydride (13.8 g, 65 mmol). After stirring for 10 minutes, acetic acid (2.9 ml, 50.7 mmol) was added via syringe over a 5 minute period. The reaction was stirred under an N2 atmosphere for 16 hrs. At the end of this period the reaction was quenched by the careful addition of a solution of saturated aqueous ammonium chloride (100 ml). After stirring for 0.5 hr, the reaction was poured over ether (250 ml) and the layers were separated. The ether layer was washed with saturated aqueous ammonium chloride (100 ml), dried (Na2SO4), filtered and evaporated in vacuo. Flash column chromatography (silica, 1:39; EtOAC:hexanes) provided N-(4'-iodophenyl)-2-aminooctane (14.6 g, 88%) as a light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05422114
Quelldatensatzuspto-grants-1995_06
ORD IDord-c9b02b03867a4d5a8003dffb26df1f7d
Quellennotizuspto-grants-1995_06