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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5,7-dichloro-4-hydroxyquinoline-2-carboxylate | HCID 14743007 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-benzyloxy-5,7-dichloroquinoline-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270309 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-24557c60eded4680bbf71a1518d52b12 |
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| Source note | uspto-grants-1993_12 |
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