Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625664Generated: October 30, 2026

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

https://huagongshe.com/reaction/1625664

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 methanol (20 mL) was added ethylamine (2M in methanol; 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 ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were dried over magnesium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (0-5% 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-096e142eb4c94005bdc8aaae818bb679
Source noteuspto-grants-2014_07