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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708537Generated: November 1, 2026

Dimethyl malonate → HCID 18959456, compound

https://huagongshe.com/reaction/1708537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl malonateHCID 7943—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 18959455HCID 18959455—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 18959456HCID 1895945648%

Reaction Conditions

Temperature57 °C

Reaction Steps

2,5-Dichloro-4-(2-[4-(t-butoxycarbonyl)-1-piperazinyl]ethyl)-nitrobenzene (5 g, 13 mmol) and dimethyl malonate (3.8 ml, 33 mmol) were stirred in N-methyl pyrrolidone (75 ml), at room temperature under nitrogen, while sodium hydride (1.33 g, 33 mmol, 60% in oil) was added. The reaction mixture was heated to 57° C. for 7 hours. The reaction mixture was cooled and poured into saturated aqueous ammonium chloride solution and extracted twice with ethyl acetate. The combined organic layers were washed with water three times, one time with brine and dried over magnesium sulfate. Evaporation of the solvent in vacuo gave an oil which was chromatographed over flash silica gel with ethyl acetate/hexanes followed by ethyl acetate. The fractions containing the desired product were combined and evaporated to give an oil, 2.5 g, 48% yield. NMR (CDCl3) δ 8.09 (s, 1), 7.45 (s, 1), 5.31 (s, 1), 3.79 (s, 6), 3.43 (m, 4), 2.98 (t, 2), 2.61 (t, 2), 2.47 (m, 4), 1.43 (s, 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359068
Source datasetuspto-grants-1994_10
ORD IDord-af5e83d173f3414387ed51cd5944be6b
Source noteuspto-grants-1994_10