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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454416Generated: October 30, 2026

Hydrochloric Acid → 2-Amino-1-(4-bromophenyl)ethanone

https://huagongshe.com/reaction/454416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexamethylenetetramineHCID 4101—
Reactant4-Bromophenacyl bromideHCID 7454—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product2-Amino-1-(4-bromophenyl)ethanoneHCID 2163992.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a stirred solution of 2-bromo-1-(4-bromophenyl)ethanone (130 g 0.478 mol) in toluene (2500 mL) was added hexamethylenetetramine (65.6 g 0.478 mol). The mixture was stirred at 40° C. for 16 hrs. The resulting solid was filtered off and washed with toluene and ether to give a white solid. To a stirred suspension of this white solid in ethanol (800 mL) was added concentrated hydrochloride acid (300 mL). The mixture was stirred at ambient temperature for 20 hrs. The solid was collected by filtration and washed with ethanol and water and dried in vacuo to give 2-amino-1-(4-bromophenyl)ethanone (4) (95 g, yield: 92%) as a white solid, which was used without purification for the next step. 1H NMR (300 MHz, DMSO-d6) δ ppm 8.58 (s, br, 2H), 7.96 (d, J=8.7 Hz, 2H), 7.81 (d, J=8.7 Hz, 2H), 4.48-4.52 (m, 2H). ES LC-MS m/z=214, 216 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492554B2
Source datasetuspto-grants-2013_07
ORD IDord-71fe715373b3405eb024d8e32d59c314
Source noteuspto-grants-2013_07