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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625672Generated: November 1, 2026

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

https://huagongshe.com/reaction/1625672

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 (15.0 g, 48.3 mmol) in methanol (60 mL) was added ethylamine (2.0M in methanol; 48 mL, 72.0 mmol), followed by acetic acid (3.0 mL, 53.4 mmol), and the mixture was stirred at room temperature for 30 minutes, after which a precipitate formed. Sodium cyanoborohydride (6.00 g, 95.4 mmol) was then added in 3 portions and the precipitate disappeared. The reaction was stirred at room temperature for 24 hours then quenched with saturated aqueous sodium bicarbonate. The resulting mixture was evaporated then diluted with dichloromethane and washed with water, dried over magnesium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (0-4% methanol in dichloromethane) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785393B2
Source datasetuspto-grants-2014_07
ORD IDord-5f82fe486a71488e898637325541a050
Source noteuspto-grants-2014_07