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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334490Generated: October 29, 2026

Sodium Bicarbonate → N-(2-nitro-6-(pyridin-2-yl)phenyl)acetamide

https://huagongshe.com/reaction/334490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Tributylstannyl)pyridineHCID 607784—
ReactantN-(2-bromo-6-nitrophenyl)acetamideHCID 4643062—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductN-(2-nitro-6-(pyridin-2-yl)phenyl)acetamideHCID 8670107092%

Reaction Steps

A degassed mixture of N-(2-bromo-6-nitrophenyl)acetamide (XCI) (4.8 g, 19 mmol, 1.00 eq), 2-(tributylstannyl)pyridine (XCVII) (7.5 g, 20 mmol, 1.05 eq) and Pd(PPh3)4 (2.1 g, 1.8 mmol, 0.01 eq) in toluene (60 mL) was heated to reflux under nitrogen overnight. Saturated sodium bicarbonate solution (50 mL) was then added to the mixture and it was extracted with ethyl acetate (50 mL×3). The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo, the residue was purified by column chromatography on silica gel (EtOAc:PE=1:2→100% EtOAc) to afford N-(2-nitro-6-(pyridin-2-yl)phenyl)acetamide (XCVIII) (4.4 g, 17.1 mmol, 92% yield) as a white-off solid. 1H NMR (DMSO-d6, 400 MHz) δ ppm 1.93 (s, 3H), 7.43-7.51 (m, 1H), 7.51-7.65 (m, 1H), 7.67 (d, J=7.6 Hz, 1H), 7.97 (dd, J=7.6 Hz, J=2.4 Hz, 3H), 8.75 (d, J=4.4 Hz, 1H), 10.52 (s, 1H); ESIMS found for C13H11N3O3 m/z 258 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883822B2
Source datasetuspto-grants-2014_11
ORD IDord-e5f180409ded43da950c7aec9f5e9216
Source noteuspto-grants-2014_11