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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690635Generated: October 31, 2026

Cesium fluoride → Ethyl 3-{3'-[(tert-butylsulfonyl)methyl]-4'-chloro-2-(3-methoxypropoxy)biphenyl-4-yl}propanoate

https://huagongshe.com/reaction/1690635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant2-{3-[(Tert-butylsulfonyl)methyl]-4-chlorophenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 66906305—
ReactantEthyl 3-[3-(3-methoxypropoxy)-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl]propanoateHCID 86633298—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 3-{3'-[(tert-butylsulfonyl)methyl]-4'-chloro-2-(3-methoxypropoxy)biphenyl-4-yl}propanoateHCID 6690656139.1%

Reaction Steps

Ethyl 3-[3-(3-methoxypropoxy)-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl]propanoate (1.1 g, 2.65 mmol) was dissolved in 1,2-dimethoxyethane (15.7 ml) and ethanol (1.5 ml). 2-{3-[(tert-butylsulfonyl)methyl]-4-chlorophenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.09 g, 2.92 mmol) was added and argon was bubbled in the solution for 10 minutes. Cesium fluoride (0.89 g, 5.84 mmol) and palladium tetrakistriphenylphosphine (0.153 g, 0.13 mmol) were: added for 2.5 hours. After cooling to room temperature, solvents were evaporated under reduced pressure and the residue was dissolved in ethyl acetate and water. The organic phase was washed with saturated aqueous ammonium chloride and brine, dried over anhydrous sodium sulphate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate, 9/1) giving 0.53 g (39%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153647B2
Source datasetuspto-grants-2012_04
ORD IDord-8c6d1f57410e41be9669c1b18d99a366
Source noteuspto-grants-2012_04