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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413704Generated: November 1, 2026

Aniline → Malonanilide

https://huagongshe.com/reaction/1413704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMalonic anhydrideHCID 10176090—
ProductMalonanilideHCID 6929872%

Reaction Steps

To the cold solution of malonic anhydride, prepared as above, was added aniline (700 μl, 6 equivalents). The reaction mixture was allowed to warm to room temperature. It was then extracted with 5 ml saturated aqueous NaHCO3, and the aqueous extract was washed with 5 ml ether, acidified with H2SO4, and extracted with 3 4-ml portions of ether. The ether extracts were combined and dried over Na2SO4, and the ether was removed under reduced pressure, to leave a residue of malonanilide (mp 127°-130° C., 180 mg, 72% isolated yield, based on diketene).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251447
Source datasetuspto-grants-1981_02
ORD IDord-473b45e1376d481dac4b2702e1df3992
Source noteuspto-grants-1981_02