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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439895Generated: November 1, 2026

Diethyl Malonate → HCID 53942467, compound

https://huagongshe.com/reaction/1439895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 19698381HCID 19698381—
SolventDimethylformamideHCID 6228—
ProductHCID 53942467HCID 5394246795.9%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a suspension of 60% sodium hydride (5.8 g, 145 mmol) in DMF (150 mL) was added diethyl malonate (26.4 mL, 175 mmol) at room temperature, while the sodium hydride was washed with dry hexane before use. The mixture was heated at 40° C. for 1.5 h, allowed to cool at room temperature and 1-nitro-4-phthalimidomethyl-2-trifluoromethanesulfonyloxybenzene (25 g, 58 mmol) was added. The mixture was stirred overnight at room temperature, poured into 3% potassium hydrogen sulfate, and extracted with a 1:1 toluene/ethyl acetate. The extract was washed successively with 5% potassium hydrogen sulfate, water, saturated aqueous sodium bicarbonate, and brine, dried over magnesium sulfate, and concentrated. The unreacted diethyl malonate was distilled out in vacuo and the residual solid was washed with 1:1 diethyl ether/hexane to give 24.5 g of the title compound: 1H NMR (CDCl3) δ8.04 (d, 1H, J=8.9 Hz), 7.85~7.90 (m, 2H), 7.72~7.78 (m, 2H), 7.56 (d, 1H, J=8.9 Hz), 7.54 (s, 1H), 5.24 (s, 1H), 4.90 (s, 2H), 4.27 (q, 4H, J=7.3 Hz), 1.28 (t, 6H, J=7.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05496843
Source datasetuspto-grants-1996_03
ORD IDord-4837f934d47542fa95e45d120a7519e8
Source noteuspto-grants-1996_03