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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033134Generated: November 2, 2026

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

https://huagongshe.com/reaction/1033134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,1-DichloroethaneHCID 6365—
Reactant2-OctanoneHCID 8093—
Reactant4-IodoanilineHCID 10893—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ProductN-(4'-iodophenyl)-2-aminooctaneHCID 992752188.2%

Reaction Steps

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-amino octane (14.6 g, 88%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310537
Source datasetuspto-grants-1994_05
ORD IDord-d41a4156190449f8b1ce9f4d061913d3
Source noteuspto-grants-1994_05