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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730382Generated: October 25, 2026

4-Bromophenacyl bromide → HCID 178441576, compound

https://huagongshe.com/reaction/730382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantPotassium CarbonateHCID 11430—
ReactantPropanimidamide, 2,2-dimethyl-, hydrochloride (1:1)HCID 2781880—
SolventDimethylformamideHCID 6228—
ProductHCID 178441576HCID 17844157681%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2,4′-dibromoacetophenone (4.17 g, 15.0 mmol) in N,N-dimethylformamide (60.0 mL) was treated with t-butylcarbamidine hydrochloride (2.05 g, 15.0 mmol) and K2CO3 (4.15 g, 30.0 mmol) and heated to 50° C. for 4 h. Following cooling, the reaction was quenched with water, diluted with brine, and extracted thrice with EtOAc. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. Purification via flash column chromatography (10-40% EtOAc/hexanes) gave the title compound as a light yellow solid (3.38 g; 81%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.58 (d, J=8.1 Hz, 2 H) 7.46 (d, J=8.6 Hz, 2 H) 7.18 (s, 1 H) 1.42 (s, 9 H). MS(ES+) m/e 279/281 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582668B2
Source datasetuspto-grants-2009_09
ORD IDord-c87a607869694ce893c90854d6234359
Source noteuspto-grants-2009_09