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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408004Generated: October 31, 2026

Sodium Bicarbonate → (2-(2-Nitro-5-(piperidin-1-yl)phenyl)pyridin-4-yl)(3-(trifluoromethyl)phenyl)methanol

https://huagongshe.com/reaction/1408004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-(2-Nitro-5-(piperidin-1-yl)phenyl)isonicotinaldehydeHCID 86705938—
ReactantHCID 178506175HCID 178506175—
SolventTetrahydrofuranHCID 8028—
Product(2-(2-Nitro-5-(piperidin-1-yl)phenyl)pyridin-4-yl)(3-(trifluoromethyl)phenyl)methanolHCID 86705939—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a −78° solution of 110 mg of 2-(2-nitro-5-(piperidin-1-yl)phenyl)isonicotinaldehyde in 4 mL of THF was added 0.82 mL of a 1.0 M solution of 3-(trifluoromethyl)phenylmagnesium chloride in THF. After 5 min the solution was warmed to 0° C. and treated with 10 mL of a saturated aqueous solution of NaHCO3. The mixture was extracted with ethyl acetate and the organic extracts were washed with water and then with brine. The solution was dried (Na2SO4) and the solvent was evaporated. The residue was purified by silica gel chromatography eluting with 1:1 ethyl acetate/hexanes to give 123 mg of product. MS (ES, m/z) 458.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916569B2
Source datasetuspto-grants-2014_12
ORD IDord-c3f9e2df443a46c89ac9055567b04e9e
Source noteuspto-grants-2014_12