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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239342Generated: October 30, 2026

Sodium hydride → HCID 68710696, compound

https://huagongshe.com/reaction/2239342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-FluorobenzonitrileHCID 67880—
Reactant1-Methyl-4-piperidinemethanolHCID 271971—
SolventDimethylformamideHCID 6228—
ProductHCID 68710696HCID 68710696—

Reaction Steps

(1-Methylpiperidin-4-yl)methanol (0.500 g, 3.87 mmol) was dissolved in dry DMF (8 mL), cooled (<0° C.), NaH (0.232 g, 5.80 mmol, 55% in oil) added and stirred for 30 minutes. 3-fluorobenzonitrile (0.492 g, 4.06 mmol) was added and the reaction mixture allowed to warm to r.t. over 1 hour. Due to excessive foaming the reaction mixture was diluted with dry DMF to 20 mL and stirred over night at r.t. The reaction was quenched by addition of water portionwise, and the mixture was extracted with EtOAc. The organics were dried (MgSO4) and concentrated in vacuo. The product was purified by flash chromatography using a step gradient of EtOAc:MeOH:TEA (100:10:2) in EtOAc to give the title compound as an oil. Yield: 0.417 g (44%). 1H NMR (400 MHz, CDCl3) δ 7.29-7.35 (m, 1H), 7.19 (m, 1H), 7.05-7.10 (m, 2H), 3.78 (d, 2H, J=6.1 Hz), 2.83-2.90 (m, 2H), 2.26 (s, 3H), 1.89-1.98 (m, 2H), 1.70-1.84 (m, 3H), 1.33-1.46 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723331B2
Source datasetuspto-grants-2010_05
ORD IDord-90df9daddb8b43b09606bcf179a0161f
Source noteuspto-grants-2010_05