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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630999Generated: November 4, 2026

Water → Methyl 3'-fluoro-2-(methoxymethyl)-2'-methylbiphenyl-4-carboxylate

https://huagongshe.com/reaction/1630999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium fluorideHCID 25953—
Reactant3-Fluoro-2-methylphenylboronic AcidHCID 2783191—
ReactantMethyl 4-bromo-3-(methoxymethyl)benzoateHCID 58554220—
CatalystHCID 178418476HCID 178418476—
Solventtert-Butyl methyl etherHCID 15413—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3'-fluoro-2-(methoxymethyl)-2'-methylbiphenyl-4-carboxylateHCID 58554131—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl 4-bromo-3-(methoxymethyl)benzoate (5.00 g, 19.3 mmol), 3-fluoro-2-methylphenylboronic acid (Combi-Blocks BB-3475, 4.46 g, 29.0 mmol), bis(triphenylphosphine)palladium(II) chloride (271 mg, 0.39 mmol) and cesium fluoride (8.79 g, 57.9 mmol) was prepared in dioxane (50 mL) and water (20 mL) under N2 atmosphere. The reaction mixture was heated at 100° C. for 1 hour. The reaction mixture was cooled at RT, diluted with MTBE (250 mL) and the layers were separated. The organic layer was washed with water (100 mL) and brine (100 mL). The aqueous layers were extracted with MTBE (150 mL). The organic layers were combined, dried (MgSO4) and concentrated under reduced pressure. After purification by flash chromatography (silica, EtOAc/n-hexane), the title compound was obtained as a colorless oil (4.85 g, 87%). HPLC (Method A), Rt: 5.0 min (purity: 99.5%). UPLC/MS, M+(ESI): 289.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791142B2
Source datasetuspto-grants-2014_07
ORD IDord-b1b5ab17e4b349daab951182c855564e
Source noteuspto-grants-2014_07