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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloro-4-nitrobenzene | HCID 7443 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dimethyl 2-(2-chloro-4-nitrophenyl)malonate | HCID 11414995 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08232283B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-b150edc1ed3e47df8a8e0a1a8d6a56a1 |
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| Source note | uspto-grants-2012_07 |
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