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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260181Generated: November 2, 2026

Sodium bis(trimethylsilyl)amide → 4-(Tetrahydro-2H-pyran-4-yl)benzonitrile

https://huagongshe.com/reaction/1260181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-Cyanophenylboronic acidHCID 2734326—
Reactant4-iodotetrahydro-2H-pyranHCID 2795506—
ReactantCyclohexanol, 2-amino-, hydrochloride (1:1), (1R,2R)-HCID 12228412—
CatalystNickel(II) iodideHCID 26038—
SolventIsopropanolHCID 3776—
Product4-(Tetrahydro-2H-pyran-4-yl)benzonitrileHCID 66632976—

Reaction Steps

186 mg (0.594 mmol) of nickel(II) iodide, 90 mg (0.594 mmol) of trans-2-aminocyclohexanol hydrochloride and 3.63 g (19.8 mmol) of sodium hexamethyldisilazide were added to a solution of 2.91 g (19.8 mmol) of 4-cyanophenylboronic acid [M. Nishimura et al., Tetrahedron 2002, 58 (29), 5779-5788] in 20 ml of isopropanol. The suspension thus obtained was stirred at RT under an argon atmosphere for 5 min. Then 2.1 g (9.90 mmol) of 4-iodotetrahydropyran [Heuberger et al., J. Chem. Soc. 1952, 910] were added. After the reaction mixture had been stirred at a temperature of 75° C. for 15 h, it was cooled to RT and substantially freed of inorganic salts with dichloromethane by filtration through approx. 50 g of silica gel. The crude product was purified by MPLC (silica gel, eluent: dichloromethane). 986 mg (53% of theory) of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470811B2
Source datasetuspto-grants-2013_06
ORD IDord-634714693c3346aaaf3b6cc97bfe5f28
Source noteuspto-grants-2013_06