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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393514Generated: October 25, 2026

Methanol → 4-Anilinophenyl 4-(4-nitrophenyl)butanoate

https://huagongshe.com/reaction/393514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-(4-Nitrophenyl)butyric acidHCID 24047—
Reactant4-HydroxydiphenylamineHCID 31208—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventDichloromethaneHCID 6344—
Product4-Anilinophenyl 4-(4-nitrophenyl)butanoateHCID 2264643789%

Reaction Steps

0.98 g (6.02 mmol) of 1,1′-carbonyldiimidazole is slowly added at 20° C. to a solution of 1.25 g (5.96 mmol) of 4-nitrophenylbutyric acid in 25 ml CH2Cl2. The reaction mixture is agitated for 30 minutes before the addition of 1 g (5.42 mmol) of 4-hydroxydiphenylamine. After agitation for 3 hours, the reaction is stopped by the addition of 3 ml of MeOH and the solvent is evaporated under vacuum. The evaporation residue is purified on a silica column (eluent: Heptane/AcOEt: 100/0 to 80/20). A yellow solid is obtained with a yield of 89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809090B2
Source datasetuspto-grants-2004_10
ORD IDord-5469ec2036f44108a9d2609512fabd9f
Source noteuspto-grants-2004_10