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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727405Generated: November 1, 2026

Diisobutylamine → 4-fluoro-N,N-diisobutyl-3-nitrobenzamide

https://huagongshe.com/reaction/1727405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylamineHCID 8085—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant4-Fluoro-3-nitrobenzoic acidHCID 67987—
SolventTetrahydrofuranHCID 8028—
Product4-fluoro-N,N-diisobutyl-3-nitrobenzamideHCID 6074915863%

Reaction Conditions

Temperature20 °C

Reaction Steps

Diisopropylcarbodiimide (13.8 ml, 1.2 eq) is added to 4-fluoro-3-nitrobenzoic acid (15 g, 1 eq) in solution in THF (150 ml). The mixture is stirred for 3 hours at a temperature of approximately 20° C. then diisobutylamine (12.9 ml, 1 eq) is added. After stirring for 15 hours at approximately 20° C., the reaction mixture is evaporated under reduced pressure at 40° C. The residue is taken up in dichloromethane (200 ml) and water (70 ml). After decantation and extraction, the combined organic phases are washed with salt water, followed by drying over Na2SO4 then evaporating under reduced pressure at 40° C. Purification of the compound by flash chromatography on silica gel (eluent: heptane/ethyl acetate 8:2) produces the expected compound in the form of a yellow solid (13.8 g; 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495110B2
Source datasetuspto-grants-2009_02
ORD IDord-6af9d179815b41d39c33e86a4420b708
Source noteuspto-grants-2009_02