Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77354Generated: October 26, 2026

Bromomethyl 4-methoxyphenyl ketone → HCID 67365424, compound

https://huagongshe.com/reaction/77354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 5-bromo-1H-pyrrole-2-carboxylateHCID 59559613—
SolventDimethylformamideHCID 6228—
ProductHCID 67365424HCID 6736542469%

Reaction Steps

A mixture of ethyl 5-bromo-1H-pyrrole-2-carboxylate (0.13 g, 0.64 mmol), 2-bromo-1-(4-methoxyphenyl)ethanone (160 mg, 0.69 mmol) and potassium carbonate (132 mg, 0.95 mmol) in N,N-dimethylformamide (4 mL) was stirred at room temperature overnight. At this time, the light brown reaction mixture was quenched with water. The resulting precipitate was collected by filtration and dried in vacuo. The resulting solid was dissolved in methylene chloride, concentrated in vacuo and then triturated with diethyl ether. The resulting solid was collected by filtration and dried in vacuo to afford 5-bromo-1-[2-(4-methoxy-phenyl)-2-oxo-ethyl]-1H-pyrrole-2-carboxylic acid methyl ester (155 mg, 69%) as light brown solid. 1H NMR (chloroform-d) δ ppm 8.00 (d, J=8.8 Hz, 2H), 6.96-7.07 (m, 3H), 6.85 (d, J=1.8 Hz, 1H), 5.71 (s, 2H), 3.91 (s, 3H), 3.75 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841299B2
Source datasetuspto-grants-2014_09
ORD IDord-835237f0d9e14a5ca87c545061af1202
Source noteuspto-grants-2014_09