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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968953Generated: October 30, 2026

Sodium hydride → Di-tert-butyl 2-(4-methyl-2-nitrophenyl)malonate

https://huagongshe.com/reaction/1968953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDi-tert-butyl malonateHCID 68324—
Reactant4-Fluoro-3-nitrotolueneHCID 136287—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductDi-tert-butyl 2-(4-methyl-2-nitrophenyl)malonateHCID 5785668429.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of di-tert-butyl malonate (1.5 mL, 6.70 mmol) in N, N-dimethylformamide (15 mL) at 0° C. under argon was treated portionwise over 10 minutes with sodium hydride (276 mg of 60% oil dispersion, 6.90 mmol) and stirred at 0° C. for 15 minutes before allowing to warm to room temperature over 1 hour. A white precipitate was produced. The stirred mixture was cooled to 0° C. and treated with a solution of 4-fluoro-3-nitrotoluene (1.0 g, 6.45 mmol) in N,N-dimethylformamide (2 mL) and a deep purple colour was immediately formed. This mixture was stirred at room temperature for 28 hours then heated at 70° C. for 6 hours. The mixture was cooled, then diluted with water (100 mL) and extracted with Et2O (2×50 mL). The combined extract was washed with water (70 mL), dried (Na2SO4) and concentrated under vacuum. The residue was purified by chromatography on silica gel (40 g) eluting with toluene to afford the title compound as a yellow oil (660 mg, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426443B2
Source datasetuspto-grants-2013_04
ORD IDord-2a660bbef6df410280773e3017029c19
Source noteuspto-grants-2013_04