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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063504Generated: November 2, 2026

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

https://huagongshe.com/reaction/2063504

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 (EDC) (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 heptane/ethyl acetate 70:30) produces the expected compound (12.36 g; 71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288395B2
Source datasetuspto-grants-2012_10
ORD IDord-fdcae4f2dd94448a9a6f38e6ca9c3bbe
Source noteuspto-grants-2012_10