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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697840Generated: November 2, 2026

4-Bromophenacyl bromide → HCID 178441576, compound

https://huagongshe.com/reaction/1697840

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 numberUS08163919B2
Source datasetuspto-grants-2012_04
ORD IDord-0a5429d6ac4a4a72b5f05949b312cce4
Source noteuspto-grants-2012_04