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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572539Generated: October 29, 2026

Water → Methyl 2'-(difluoromethyl)-2-methylbiphenyl-4-carboxylate

https://huagongshe.com/reaction/572539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium fluorideHCID 25953—
Reactant1-Bromo-2-(difluoromethyl)benzeneHCID 2761181—
Reactant2-Methyl-4-methoxycarbonylphenylboronic acid, pinacol esterHCID 11087024—
CatalystHCID 178418476HCID 178418476—
Solventtert-Butyl methyl etherHCID 15413—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 2'-(difluoromethyl)-2-methylbiphenyl-4-carboxylateHCID 66653005—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of methyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (Combiblocks PN-8756, 1.9 g, 6.7 mmol), 1-bromo-2-difluoromethyl-benzene (Fluorochem 023878, 1.7 g, 8.1 mmol), cesium fluoride (3.1 g, 20 mmol) and PdCl2(PPh3)2 (142 mg, 0.20 mmol) was prepared in dioxane (20 mL) and water (10 mL) under N2 atmosphere. The resulting mixture was heated at 90° C. for 2 hours. The reaction mixture was diluted with MTBE (60 mL), and then washed with water (2×50 mL) and brine (50 mL). The aqueous layers were extracted with MTBE (50 mL). The organic layers were combined, dried (MgSO4) and concentrated under reduced pressure. After purification by flash chromatography (silica, DCM/heptane), the title compound was obtained as a colorless oil (1.4 g, 76%). HPLC (Method A) Rt 5.0 min (purity: 99.1%). 1H NMR (DMSO-d6, 300 MHz) δ 7.93 (s, 1H), 7.84 (dd, J=7.9, 1.4 Hz, 1H), 7.75 (m, 1H), 7.67-7.56 (m, 2H), 7.28 (m, 2H), 6.55 (t, J=55 Hz, 1H), 3.88 (s, 3H), 2.06 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029405B2
Source datasetuspto-grants-2015_05
ORD IDord-9f7927c6708c494ca6fcdbca3d334aa6
Source noteuspto-grants-2015_05