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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517248Generated: November 4, 2026

1,2-Dichloro-4-nitrobenzene → Dimethyl 2-(2-chloro-4-nitrophenyl)malonate

https://huagongshe.com/reaction/1517248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dichloro-4-nitrobenzeneHCID 7443—
ReactantDimethyl malonateHCID 7943—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductDimethyl 2-(2-chloro-4-nitrophenyl)malonateHCID 1141499574%

Reaction Steps

NaH (288 mmol) was suspended in DMF (370 mL) at 0° C. under an atmosphere of nitrogen. Dimethyl malonate (261 mmol) in DMF (30 mL) was added dropwise over a period of 20 min. at 0° C. and stirring was continued at 0° C. for 30 min. Then 1,2-dichloro-4-nitrobenzene (130 mmol) in DMF (35 mL) was added dropwise at 0° C. over a period of 20 min. The mixture was stirred at 70° C. for 15 h. The reaction mixture was cooled to room temperature and quenched with NH4Cl. The solution was successively washed with EtOAc (1×100 mL, 1×250 mL) and water (2×150 mL). To facilitate separation of the layers, sat. aq. NaCl (20 mL) was added. The organic layer was separated and washed with sat. aq. NaCl (2×100 mL). The aqueous layer was backextracted with EtOAc (2×50 mL). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material was recrystallized from EtOH to give dimethyl 2-(2-chloro-4-nitrophenyl)malonate as a solid (74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232283B2
Source datasetuspto-grants-2012_07
ORD IDord-b150edc1ed3e47df8a8e0a1a8d6a56a1
Source noteuspto-grants-2012_07