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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889764Generated: October 30, 2026

(1,1'-Binaphthalen)-2-yldi-tert-butylphosphine → HCID 57666005, compound

https://huagongshe.com/reaction/889764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
ReactantHCID 3595928HCID 3595928—
ReactantSodium t-butoxideHCID 23676156—
Reactant4-Methyl-2-(5-trifluoromethanesulfonyloxy-4'-trifluoromethyl-biphenyl-3-yl)-pentanoic acid ethyl esterHCID 57755055—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 57666005HCID 57666005—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-methyl-2-(5-trifluoromethanesulfonyloxy-4′-trifluoromethyl-biphenyl-3-yl)-pentanoic acid ethyl ester (1g) (190 mg, 0.37 mmol) in toluene (2.5 mL) in a sealed tube was added racemic-2-(di-t-butylphosphino)-1,1′-binaphthyl (44 mg, 0.11 mmol), Pd(OAc)2 (83 mg, 0.37 mmol), 2-(2-methyl-benzyl)-piperidine (98 mg, 0.52 mmol). The system was flushed with nitrogen. To this was added NaOtBu (53 mg, 0.56 mmol) and heated to 100° C. for 1 h. The reaction was cooled to room temperature and quenched by slow addition of water. The mixture was extracted with EtOAc (3×20 mL). The organic phase was washed with saturated NaHCO3 solution and brine. The organic fraction was dried (MgSO4) and concentrated in vacuo. The crude mixture was purified by ISCO column chromatography to obtain 4-methyl-2-{5-[2-(2-methyl-benzyl)-piperidin-1-yl]-4′-trifluoromethyl-biphenyl-3-yl}-pentanoic acid ethyl ester. Calcd for C34H40F3NO2 (M+H) 552.68, Found 552.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252935B2
Source datasetuspto-grants-2012_08
ORD IDord-13e223d679194c3c94918b2066c2022f
Source noteuspto-grants-2012_08