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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621260Generated: November 2, 2026

4-Bromophenacyl bromide → HCID 178441576, compound

https://huagongshe.com/reaction/1621260

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, 2H) 7.46 (d, J=8.6 Hz, 2H) 7.18 (s, 1H) 1.42 (s, 9H). MS (ES+) m/e 279/281 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772507B2
Source datasetuspto-grants-2014_07
ORD IDord-3ee2924311db40f19a59b92c9172d20a
Source noteuspto-grants-2014_07