Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686857Generated: November 3, 2026

Sodium Bicarbonate → 4-Iodo-2-nitrobenzaldehyde

https://huagongshe.com/reaction/1686857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Bromomethyl)-4-iodo-2-nitrobenzeneHCID 17966024—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-Iodo-2-nitrobenzaldehydeHCID 2153278561%

Reaction Conditions

Temperature86 °C

Reaction Steps

NaHCO3 (3.32 g, 39.48 mmol) was added to a solution of 1-bromomethyl-4-iodo-2-nitrobenzene (2.25 g, 6.58 mmol) in anhydrous DMSO (150 mL). The mixture was stirred at 86° C. for 19 hours under a nitrogen atmosphere, then cooled down to room temperature, diluted with water (300 mL), and extracted with methylene chloride four times (250 mL). The combined organic phase was dried over Na2SO4, concentrated in vacuo, and purified by silica gel chromatography to yield 4-iodo-2-nitrobenzaldehyde (1.11 g, 61%). 1H NMR (400 MHz, CDCl3): δ 10.38 (d, 1H, J=1.6 Hz, CHO), 8.45 (d, 1H, J=1.5 Hz, Ph-H), 8.15 (dd, 1H, J=1.5 and 8.0 Hz, Ph-H), 7.67 (d, 1H, J=8.1 Hz, Ph-H); 13C NMR (100 MHz, CDCl3): δ 187.28 (CH), 143.18 (CH), 133.29 (CH), 130.67 (CH), 130.28 (C), 109.60 (C), 99.78 (C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148503B2
Source datasetuspto-grants-2012_04
ORD IDord-66183504377242d0bb32ec16048286eb
Source noteuspto-grants-2012_04