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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82030Generated: October 26, 2026

Acetic Acid → N-(3-Iodobenzyl)-N,N-dimethylamine

https://huagongshe.com/reaction/82030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylacetamideHCID 31374—
Reactant3-IodobenzaldehydeHCID 252610—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
ProductN-(3-Iodobenzyl)-N,N-dimethylamineHCID 1775032190%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 3-iodo-benzaldehyde (3 g, 12.9 mmol) in anhydrous dichloromethane (130 ml) were added acetic acid (1.9 ml) and N,N-dimethylacetamide. The yellow solution is stirred 10 minutes at 0° C. and sodium triacetoxyborohydride (6.85 g, 32.33 mmoles) is added by portions. The resulting mixture is stirred at room temperature for 90 minutes and evaporated to dryness under reduced pressure. Ethyl acetate and a saturated aqueous hydrogen carbonate solution were added to the residue and the two layers were separated The organic phase was washed with water, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to yield (3-iodo-benzyl)-dimethyl-amine (3.05 g, 90%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846712B2
Source datasetuspto-grants-2014_09
ORD IDord-f043558804914f0eaa1eb00ec10c1e75
Source noteuspto-grants-2014_09