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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 4-Cyanophenylboronic acid | HCID 2734326 | — |
| Reactant | 4-iodotetrahydro-2H-pyran | HCID 2795506 | — |
| Reactant | Cyclohexanol, 2-amino-, hydrochloride (1:1), (1R,2R)- | HCID 12228412 | — |
| Catalyst | Nickel(II) iodide | HCID 26038 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(Tetrahydro-2H-pyran-4-yl)benzonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470811B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-634714693c3346aaaf3b6cc97bfe5f28 |
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| Source note | uspto-grants-2013_06 |
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