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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372606Generated: October 25, 2026

Hydrochloric Acid → Di-tert-butyl (3-fluoro-4-nitrophenyl)malonate

https://huagongshe.com/reaction/1372606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant2,4-DifluoronitrobenzeneHCID 67967—
ReactantDi-tert-butyl malonateHCID 68324—
SolventTetrahydrofuranHCID 8028—
ProductDi-tert-butyl (3-fluoro-4-nitrophenyl)malonateHCID 6740743113.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

In THF (400 ml) were dissolved 2,4-difluoronitrobenzene (17.4 g, 109 mmol) and di-tert-butyl malonate (27.0 ml, 120 mmol). Under stirring at 0° C., sodium hydride (60% in oil, 4.82 g, 120 mmol) was added in portions. The reaction mixture was then stirred overnight at room temperature. The reaction mixture was poured in 1.0N-HCl (300 ml), followed by extraction with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from hexane-ethyl acetate (20:1 to 10:1) eluate fractions, di-tert-butyl (3-fluoro-4-nitrophenyl)malonate (5.17 g, 13%) was obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-3c7d02f449d74491a5c4769793bb2997
Source noteuspto-grants-2007_01