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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372571Generated: October 30, 2026

Sodium hydride → HCID 67406367, compound

https://huagongshe.com/reaction/1372571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDi-tert-butyl malonateHCID 68324—
Reactant1-Benzyloxy-2,3-difluoro-6-nitrobenzeneHCID 17858881—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67406367HCID 6740636795%

Reaction Conditions

Temperature0 °C

Reaction Steps

In THF (100 ml) were dissolved 1-benzyloxy-2,3-difluoro-6-nitrobenzene (4.17 g, 15.7 mmol) and di-tert-butyl malonate (3.52 ml, 15.7 mmol). To the resulting solution was added sodium hydride (60% in oil, 1.26 g, 31.4 mmol) in portions under stirring at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes and then at 80° C. for 9 hours. Di-tert-butyl malonate (7.04 ml, 31.4 mmol) and sodium hydride (60%; 2.52 g, 52.8 mmol) were added and the mixture was stirred at 80° C. for 2 days. After cooling to room temperature, the reaction mixture was poured in ice water (100 ml), followed by extraction with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (silica gel: 200 g), whereby from hexane/ethyl acetate (8/1) eluate fractions, the title compound (6.87 g, 95%) was obtained as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-7382b9ba0194474fa0ba36968a85abfa
Source noteuspto-grants-2007_01