HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883679Generated: October 30, 2026
Diisobutylamine → 4-fluoro-N,N-diisobutyl-3-nitrobenzamide
https://huagongshe.com/reaction/883679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylamine | HCID 8085 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 4-Fluoro-3-nitrobenzoic acid | HCID 67987 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-fluoro-N,N-diisobutyl-3-nitrobenzamide | HCID 60749158 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236965B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-5f67905f78734948a28580205e21eda2 |
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| Source note | uspto-grants-2012_08 |
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