HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → Malonanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Malonic anhydride | HCID 10176090 | — |
| Product | Malonanilide | HCID 69298 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251447 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-473b45e1376d481dac4b2702e1df3992 |
| Source note | uspto-grants-1981_02 |