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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333460Generated: October 30, 2026

Sodium Bicarbonate → 4-Iodo-2-nitrobenzaldehyde

https://huagongshe.com/reaction/333460

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 numberUS08877905B2
Source datasetuspto-grants-2014_11
ORD IDord-1ebb7e0662fd4d42a6223b7b34fe5d78
Source noteuspto-grants-2014_11