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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889699Generated: October 31, 2026

Benzyl Bromide → HCID 57666027, compound

https://huagongshe.com/reaction/889699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57665930HCID 57665930—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 57666027HCID 57666027—

Reaction Conditions

Temperature150 °C

Reaction Steps

4-Methyl-2-[4′-trifluoromethyl-5-(6-trifluoromethyl-piperidin-2-yl)-biphenyl-3-yl]-pentanoic acid ethyl ester, compound 7b (32 mg, 0.062 mmol), Benzyl bromide (55 μl, 0.46 mmol), DIEA (110 μl, 0.62), and tetrabutylammonium iodide (TBAI)(10 mg) in acetonitrile (0.5 mL) were combined and heated under microwave conditions 150° C. for 30 minutes. The reaction was diluted with EtOAc, washed with brine, sat. NaHCO3, and brine, dried over magnesium sulfate and filtered. Purification by silica gel chromatography gave the product as yellow oil. (56 mg, quant.) (M+H) 605.65, Found 606.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252935B2
Source datasetuspto-grants-2012_08
ORD IDord-e4e62442f2ab457faf815cd65e9d5fdb
Source noteuspto-grants-2012_08