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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456316Generated: October 29, 2026

Sodium Bicarbonate → 4-Iodo-2-nitrobenzaldehyde

https://huagongshe.com/reaction/456316

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%). 1HNMR (400 MHz, CDCl3): δ 10.38 (d, 1 H, J=1.6 Hz, CHO), 8.45 (d, 1 H, J=1.5 Hz, Ph-H), 8.15 (dd, 1 H, J=1.5 and 8.0 Hz, Ph-H), 7.67 (d, 1 H, 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 numberUS08497360B2
Source datasetuspto-grants-2013_07
ORD IDord-cf31a7c7c09949bb88fb4f87c6761234
Source noteuspto-grants-2013_07