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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 3-Iodobenzaldehyde | HCID 252610 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-Iodobenzyl)-N,N-dimethylamine | HCID 17750321 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846712B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-f043558804914f0eaa1eb00ec10c1e75 |
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| Source note | uspto-grants-2014_09 |
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