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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410472Generated: November 1, 2026

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

https://huagongshe.com/reaction/2410472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant3-Fluoro-2-methylphenylboronic AcidHCID 2783191—
Reactant3'-Fluoro-2-(methoxymethyl)-2'-methylbiphenyl-4-carboxylic acidHCID 58066398—
ReactantMethyl 4-bromo-3-(methoxymethyl)benzoateHCID 58554220—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
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 (Intermediate 1, Step 2, 5.00 g, 19.3 mmol), 3-fluoro-2-methylphenylboronic acid (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 nitrogen 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 over 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%). LC/MS (Method B): 289.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815919B2
Source datasetuspto-grants-2014_08
ORD IDord-0cf5d2f1c2c84bc3b2a455209f39cd07
Source noteuspto-grants-2014_08