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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375285Generated: October 31, 2026

P-Phenylenediamine → N-(4-aminophenyl)butanamide

https://huagongshe.com/reaction/1375285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-PhenylenediamineHCID 7814—
Reactant4-MethylmorpholineHCID 7972—
ReactantButyryl chlorideHCID 8855—
SolventDichloromethaneHCID 6344—
ProductN-(4-aminophenyl)butanamideHCID 72113137.6%

Reaction Steps

To a solution of 1,4-phenylenediamine (0.5 g, 4.62 mmol) in anhydrous CH2Cl2 (15 mL) was added NMM (0.51 mL, 4.62 mmol). To the resulting mixture was added dropwise butyryl chloride (0.45 mL, 4.62 mmol) in anhydrous CH2Cl2 (5 mL) at 0° C., and stirred for 0.5 h. The reaction mixture was extracted with CH2Cl2 (20 mL) and washed with H2O (20 mL). The organic layer was dried over MgSO4 and evaporated in vacuo. The residue was purified by column chromatography over silica gel (EtOAc:hexane=1:3) to give N-(4-aminophenyl)butyramide (KYJ3-006-2, 0.31 g, 36%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166744B2
Source datasetuspto-grants-2007_01
ORD IDord-92c9587a25624274ba059df954d064ff
Source noteuspto-grants-2007_01