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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Difluoronitrobenzene | HCID 67967 | — |
| Reactant | Di-tert-butyl malonate | HCID 68324 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Di-tert-butyl (3-fluoro-4-nitrophenyl)malonate | HCID 67407431 | 13.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-3c7d02f449d74491a5c4769793bb2997 |
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| Source note | uspto-grants-2007_01 |
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