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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326650Generated: October 29, 2026

Water → Methyl 4-benzyloxy-5,7-dichloroquinoline-2-carboxylate

https://huagongshe.com/reaction/326650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5,7-dichloro-4-hydroxyquinoline-2-carboxylateHCID 14743007—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-benzyloxy-5,7-dichloroquinoline-2-carboxylateHCID 19735155—

Reaction Steps

To a suspension of methyl 5,7-dichloro-4-oxo-1,4-dihydroquinoline-2-carboxylate (3 g) in dry dimethyl-formamide (20 ml) was added potassium carbonate (6.1 g) followed by benzyl bromide (1.44 ml) and the mixture stirred at room temperature for 16 hours. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (3×100 ml), the organic layers were combined and washed with water (2×100 ml), 1M hydrochloric acid (1×100 ml), brine (2×100 ml) and dried over magnesium sulphate. The solvent was removed under reduced pressure and the crude product purified by column chromatography to give methyl 4-benzyloxy-5,7-dichloroquinoline-2-carboxylate (2.8 g). δ (360 MHz, DMSO-d6) 3.95 (3H, s, OCH3), 5.48 (2H, s, CH2), 7.35 (1H, d, p-ArH), 7.38 (2H, t, m-ArH), 7.46 (2H, d, o-ArH), 7.59 (1H, s, 3-H), 7.83 (1H, d, 6-H) and 8.11 (1H, d, 8-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270309
Source datasetuspto-grants-1993_12
ORD IDord-24557c60eded4680bbf71a1518d52b12
Source noteuspto-grants-1993_12