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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533543Generated: October 31, 2026

2-Iodophenol → HCID 86668768, compound

https://huagongshe.com/reaction/533543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodophenolHCID 10784—
ReactantCesium fluorideHCID 25953—
Reactant5-(5-Bromopyridin-2(1H)-ylidene)-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 57443498—
Reactant2-methanesulfonyl-2-methyl-N-(tetrahydro-pyran-2-yloxy)-4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-butyramideHCID 76445394—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86668768HCID 86668768—

Reaction Conditions

Temperature115 °C

Reaction Steps

To a flask containing 2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]butanamide prepared as in Preparation Number 3 (150 mg, 0.312 mmol) was added 2-iodophenol (89.3 mg, 0.406 mmol), cesium fluoride (190 mg, 1.25 mmol), water (500 uL) and 1,4-dioxane (3 mL). To this mixture was added Palladium tetrakis (54.3 mg, 0.047 mmol) and the mixture was heated to 115° C. with stirring overnight. The mixture was diluted with ethyl acetate and water. The phases were separated and the crude organic extract was concentrated in vacuo to dryness. The crude material was purified via silica gel chromatography eluting with ethyl acetate/heptanes to afford 4-(2′-hydroxybiphenyl-4-yl)-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide as solid. 19.6 mg LCMS: (M−1) 446.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853258B2
Source datasetuspto-grants-2014_10
ORD IDord-0e2a7591f8aa451d900ec777da5c4044
Source noteuspto-grants-2014_10