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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445478Generated: October 29, 2026

1,4-Cyclohexadiene → N-(4-Fluorophenyl)-N'-(4-hydroxyphenyl)cyclopropane-1,1-dicarboxamide

https://huagongshe.com/reaction/445478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexadieneHCID 12343—
ReactantCyclopropane-1,1-dicarboxylic acid (4-benzyloxy-phenyl)-amide (4-fluoro-phenyl)-amideHCID 57810288—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-(4-Fluorophenyl)-N'-(4-hydroxyphenyl)cyclopropane-1,1-dicarboxamideHCID 5781019796.9%

Reaction Steps

To a refluxing mixture of cyclopropane-1,1-dicarboxylic acid (4-benzyloxy-phenyl)-amide (4-fluoro-phenyl)-amide (46 g, 113 mmol), 10% Pd/C (2 g) in EtOH (400 mL) was added dropwise 1,4-cyclohexadiene (62.7 mL, 678 mmol). Stirring was continued for 2-5 h until the reaction was complete. The mixture was cooled to rt, filtered through celite, and washed with EtOH. The solution was then concentrated under reduced pressure. To the flask containing the crude product was added CHCl3 (200 mL). The resulting suspension was stirred for 15 min at rt. The solid was filtered, and dried in the air to give cyclopropane-1,1-dicarboxylic acid (4-fluoro-phenyl)-amide(4-hydroxy-phenyl)-amide (34.4 g, 95%, yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476298B2
Source datasetuspto-grants-2013_07
ORD IDord-85f26bebf3224db58debca73eec7d0ae
Source noteuspto-grants-2013_07