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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523953Generated: October 25, 2026

Methyl iodide → Methyl 5-bromoquinoline-8-carboxylate

https://huagongshe.com/reaction/523953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromoquinoline-8-carboxylic acidHCID 59292860—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-bromoquinoline-8-carboxylateHCID 71607288—

Reaction Conditions

Temperature45 °C

Reaction Steps

K2CO3 (61.3 g, 444.0 mmol) and methyl iodide (63.1 g, 444.0 mmol) were added to a stirred suspension of 5-bromoquinoline-8-carboxylic acid (28.0 g, 111.0 mmol) in DMF (250 mL) at r.t. The reaction mixture was heated at 45° C. for 36 h, cooled to r.t, filtered the solids, washed with ethyl acetate (100 mL). The filtrate was diluted with water, extracted with ethyl acetate (3×300 mL) and washed with water (3×100 mL). The ethyl acetate layer was dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with ethyl acetate in hexanes (0-20%) to afford methyl-5-bromoquinoline-8-carboxylate as a cream color solid (20.5 g, 70% for 2 steps). 1H NMR (400 MHz, CDCl3) δ 9.07 (dd, J=4.3, 1.5 Hz, 1H), 8.60 (dd, J=8.7, 1.6 Hz, 1H), 7.88 (s, 2H), 7.58 (dd, J=8.6, 4.0 Hz, 1H), 4.05 (s, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340509B2
Source datasetuspto-grants-2016_05
ORD IDord-2b388fa14944469099f1af67ad49028f
Source noteuspto-grants-2016_05