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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691871Generated: October 25, 2026

Ethanol → trans-2-(4'-Amino-biphenyl-4-carbonyl)-cyclopentanecarboxylic acid

https://huagongshe.com/reaction/1691871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant(4-Aminophenyl)boronic acid hydrochlorideHCID 2734614—
Reactanttrans-2-(4-Bromobenzoyl)cyclopentanecarboxylic acidHCID 23549251—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,2-DimethoxyethaneHCID 8071—
Producttrans-2-(4'-Amino-biphenyl-4-carbonyl)-cyclopentanecarboxylic acidHCID 5765203764.6%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 4-aminophenylboronic acid hydrochloride (0.21 g, 1.2 mmol), trans-2-(4-bromo-benzoyl)-cyclopentanecarboxylic acid (0.30 g, 1 mmol), tetrakis(triphenylphosphine) palladium (0) (10 mg), 2 M aqueous sodium carbonate solution (0.5 mL), ethanol (2 mL), and ethylene glycol dimethyl ether (3 mL) was heated under microwave condition to 160° C. for 30 min. The crude reaction mixture was adsorbed onto silica gel and flash chromatography (eluting with ethyl acetate and hexanes) yielded 0.2 g of trans-2-(4′-amino-biphenyl-4-carbonyl)-cyclopentanecarboxylic acid as a brown solid. LCMS calcd for C19H19NO3 (m/e) 309, obsd 310 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153644B2
Source datasetuspto-grants-2012_04
ORD IDord-591bdc8a4b1e47b7ac2f3f7ebe21b422
Source noteuspto-grants-2012_04