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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919977Generated: October 31, 2026

Acetic Acid → (5-Bromo-2-iodo-benzyl)-ethyl-amine

https://huagongshe.com/reaction/1919977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthylamineHCID 6341—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-Bromo-2-iodobenzaldehydeHCID 21973861—
SolventMethanolHCID 887—
Product(5-Bromo-2-iodo-benzyl)-ethyl-amineHCID 58148919—

Reaction Steps

To 5-bromo-2-iodo-benzaldehyde (5.0 g, 16.1 mmol) in MeOH (20 mL) was added ethylamine (2M in MeOH; 16 mL, 24.0 mmol), followed by acetic acid (1.0 mL, 17.8 mmol), and the mixture was stirred at room temperature for 30 minutes. Sodium cyanoborohydride (2.0 g, 31.8 mmol) was then added over 5 minutes, and the reaction was stirred at room temperature over the weekend. The mixture was concentrated and partitioned between EtOAc and saturated aqueous NaHCO3. The aqueous layer was extracted with EtOAc, and the combined organic layers were dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel chromatography (0-5% MeOH in CH2Cl2) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168678B2
Source datasetuspto-grants-2012_05
ORD IDord-b0aaf92cab3f49a0b7e95a3278ac2a73
Source noteuspto-grants-2012_05