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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888361Generated: October 31, 2026

Triethylamine → HCID 68502348, compound

https://huagongshe.com/reaction/888361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 5-bromo-2'-fluoro-4'-methylbiphenyl-3-carboxylateHCID 68499851—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthanolHCID 702—
ProductHCID 68502348HCID 68502348693.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

To Biotage Advancer MW reactor was charged methyl 5-bromo-2′-fluoro-4′-methylbiphenyl-3-carboxylate (20 g, 61.9 mmol), PdCl2(dppf) (0.20 g, 0.273 mmol), potassium vinyl trifluoroborate (12.4 g, 93 mmol), Et3N (13.0 ml, 93 mmol) and EtOH (150 ml). The reactor was sealed and heated at 140° C. for 10 min followed by flash cooling. Removed mixture from the cooling reservoir via vacuum and reaction repeated 5× (120 g, 371 mmol processed). All runs were combined and concentrated to dryness. The crude was partitioned between water and dichloromethane. The layers were separated and the aqueous extracted 2× w/DCM. The combined organic layers were dried over Na2SO4, filtered and concentrated via rotary evaporation to give 116 g amber oil. The crude was purified by automated silica gel chromatography (750 g SiO2, EtOAc/hexanes) to give nearly colorless oil which solidified to white solid upon cooling (99.7 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-27529e07d86a4f52af94ab730c30f398
Source noteuspto-grants-2012_08