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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281002Generated: October 30, 2026

Methyl iodide → Methyl 5-bromoquinoline-8-carboxylate

https://huagongshe.com/reaction/2281002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromoquinoline-8-carboxylic acidHCID 59292860—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-bromoquinoline-8-carboxylateHCID 7160728814.5%

Reaction Steps

To a solution of 5-Bromoquinoline-8-carboxylic acid (30 g, 0.119 mol, crude) in DMF (400 ml) was added potassium carbonate (41.12 g, 0.297 mol) and MeI (22.3 ml, 0.357 mol) at RT. The reaction mixture was stirred at RT for 12 h and the reaction completion was confirmed by TLC. After completion of reaction the reaction mixture was filtered and evaporated. The reaction mixture was basified with 10% NaHCO3 and extracted with ethyl acetate. The organic layer was washed with water, brine and dried over sodium sulphate and concentrated to afford the title compound as brown liquid (4.6 g). LCMS: Mass found (M+, 268). 1H NMR (DMSO-d6 400 MHz): δ 9.04-9.02 (dd, J=3.92, 5.68, Hz, 1H), 8.58-8.56 (m, 1H), 8.05-8.03 (d, J=7.72 Hz, 1H), 7.87-7.86 (d, J=7.76 Hz, 1H), 7.78-7.75 (dd, J=8.6, 12.8 Hz, 1H), 3.91 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139568B2
Source datasetuspto-grants-2015_09
ORD IDord-7b3c245f13774157925e73d63e9fa9e5
Source noteuspto-grants-2015_09