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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358442Generated: November 1, 2026

Diisoamylamine → 3-fluoro-N,N-bis(3-methylbutyl)-4-nitrobenzamide

https://huagongshe.com/reaction/2358442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisoamylamineHCID 10988—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Fluoro-4-nitrobenzoic acidHCID 230653—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
Product3-fluoro-N,N-bis(3-methylbutyl)-4-nitrobenzamideHCID 6844711171%

Reaction Conditions

Temperature20 °C

Reaction Steps

1-hydroxybenzotriazole (HOBt) (8 g, 1.1 eq) in solution in THF (60 ml) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (ED)C) (11.4 g, 1.1 eq) in solution in chloroform (60 ml) are added successively to 3-fluoro-4-nitrobenzoic acid (10 g, 1 eq) in solution in anhydrous THF (60 ml). The mixture is stirred for 2 hours at a temperature of approximately 20° C. then diisoamylamine (12.2 ml, 1.1 eq) is added. After stirring for 4 hours at a temperature of approximately 20° C., the reaction mixture is concentrated under reduced pressure at 40° C. The residue is taken up in dichloromethane (300 ml) and water (100 ml). After decantation and extractions, the combined organic phases are washed with salt water, dried over Na2SO4 then concentrated under reduced pressure at 40° C. Purification by flash chromatography on silica gel (eluent: heptane 100% to heptanel ethyl acetate 70:30) produces the expected compound (12.36 g; 71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763725B2
Source datasetuspto-grants-2010_07
ORD IDord-8eeb72513e19450698fa15766c76d13d
Source noteuspto-grants-2010_07