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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404335Generated: October 27, 2026

Water → Methyl 2-chloro-2'-(trifluoromethyl)biphenyl-4-carboxylate

https://huagongshe.com/reaction/2404335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzene, 1-bromo-2-(trifluoromethyl)-HCID 9806—
ReactantCesium fluorideHCID 25953—
Reactant2-Chloro-4-(methoxycarbonyl)benzeneboronic acidHCID 22171291—
CatalystHCID 178418476HCID 178418476—
Solventtert-Butyl methyl etherHCID 15413—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 2-chloro-2'-(trifluoromethyl)biphenyl-4-carboxylateHCID 66718347—

Reaction Steps

A mixture of methyl 4-borono-3-chlorobenzoate (Combi-Blocks BB-3530, 1.5 g, 7.0 mmol), 2-bromobenzotrifluoride (1.9 g, 8.4 mmol), cesium fluoride (3.2 g; 21.0 mmol) and bis(triphenylphosphine)palladium(II) chloride (98 mg, 0.14 mmol) was prepared in dioxane (15 mL) and water (7.5 mL) under nitrogen atmosphere, and then heated at 90° C. for 30 minutes. The reaction mixture was diluted with MTBE (30 mL) and washed with water and brine. The aqueous layers were extracted with MTBE (30 mL). The combined organic layers were dried (MgSO4) and concentrated under vacuum. After two purifications by flash chromatography (silica, heptane/DCM, then heptane/EtOAc), the title compound was obtained as a yellow oil. HPLC (Method A) Rt 5.3 min (Purity: 99.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802704B2
Source datasetuspto-grants-2014_08
ORD IDord-33f9a1668d9d4ee08d656e807ae48687
Source noteuspto-grants-2014_08