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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870988Generated: October 30, 2026

Acetic Acid → 2-(Methoxy(4-nitrophenyl)methylene)malononitrile

https://huagongshe.com/reaction/870988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant2-[Hydroxy(4-nitrophenyl)methylene]malononitrileHCID 85842793—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-(Methoxy(4-nitrophenyl)methylene)malononitrileHCID 12862262—

Reaction Steps

3-Hydroxy-3-(4-nitrophenyl)-2-cyanoacrylonitrile (21.5 g, 0.10 mol) was dissolved in acetonitrile (430 mL) and of methanol (43 mL) in a flask equipped with a dropping funnel, a thermometer, a stir bar, and argon atmosphere. The flask was immersed in a −15° C. bath to the level that the internal temperature was maintained between −5° C. and 0° C. (75 mL of a 2.0 M solution in diethyl ether, 0.15 mol) was added dropwise over 20 min. HPLC analysis showed incomplete reaction, and an additional portion (25 mL, 0.05 mol) of trimethylsilyldiazomethane solution was added. This was repeated with 35 mL (0.07 mol). After 20 min, the mixture was poured into a rapidly-stirred solution of acetic acid (15 g, 0.25 mol) in EtOAc (1.8 L). The mixture was extracted with water (3×1.5 L), filtered through phase separation paper, and concentrated in vacuo. the solid residue weighed 14.4 g and was used in the next step without further purification. NMR (60 MHz) (CDCl3) δ 8.0 (AB, 4H); 4.0 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969583B2
Source datasetuspto-grants-2015_03
ORD IDord-5756305685d74e369efceaa579128456
Source noteuspto-grants-2015_03