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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846036Generated: November 3, 2026

Cesium carbonate → 5'-Bromo-4-(ethylsulfonyl)-2,2'-dimethoxy-1,1-biphenyl

https://huagongshe.com/reaction/1846036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-Bromo-2-iodo-1-methoxybenzeneHCID 10979904—
Reactant2-(4-(Ethylsulfonyl)-2-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 86723208—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
Product5'-Bromo-4-(ethylsulfonyl)-2,2'-dimethoxy-1,1-biphenylHCID 8672325945%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 4-bromo-2-iodo-1-methoxybenzene (Preparation 57, 350 mg, 1.12 mmol), 2-(4-(ethylsulfonyl)-2-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (Preparation 21, 365 mg, 1.12 mmol) and aqueous caesium carbonate solution (1M, 2.23 mL, 2.23 mmol) in dioxane (18 mL) was degassed with nitrogen for 10 min, followed by addition of 1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride (46.0 mg, 0.0056 mmol). The resulting mixture was heated at 80° C. for 16 hours. After cooling to room temperature and concentration in vacuo, the crude residue was partitioned between water (30 mL) and EtOAc (30 mL). The aqueous layer was extracted with EtOAc (2×20 mL). The organic layers were combined and washed with brine (25 mL), dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with heptanes/EtOAc (70:30), to afford the title compound as off-white solid in 45% yield, 150 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952008B2
Source datasetuspto-grants-2015_02
ORD IDord-0e5d24f2ee2444a9a172268d609a667d
Source noteuspto-grants-2015_02