HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403691Generated: November 3, 2026
Stannous chloride dihydrate → Ethyl 6-bromoquinoline-3-carboxylate
https://huagongshe.com/reaction/2403691
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Ethyl 3,3-diethoxypropionate | HCID 66389 | — |
| Reactant | 5-Bromo-2-nitrobenzaldehyde | HCID 97233 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 6-bromoquinoline-3-carboxylate | HCID 12034638 | 60% |
Reaction Steps
To a solution of 5-bromo-2-nitrobenzaldehyde (2 g, 9 mmol) in ethanol (46 mL) was added tin(II) chloride dihydrate (7.95 g, 35.2 mmol) and 3,3-diethoxypropionic acid ethyl ester (4.2 mL, 22 mmol). The reaction was heated to 90° C. for 16 hours. The reaction was then allowed to cool to room temperature and stir overnight. The reaction mixture was concentrated and the residue was dissolved in ethyl acetate. The mixture was poured into saturated aqueous sodium bicarbonate. The resulting emulsion was filtered through Celite, rinsing with ethyl acetate. The layers were separated and the aqueous was extracted with ethyl acetate. The combined organics were washed with brine, dried over magnesium sulfate, filtered, and concentrated. Purification by flash column chromatography (0-50% ethyl acetate/heptanes) gave the title compound (1.41 g, 60%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802688B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-ed06eb1e47834546948f5d1cd4f5caa0 |
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| Source note | uspto-grants-2014_08 |
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