HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258515Generated: November 2, 2026
Hydrochloric Acid → 7-Chloro-2-(2-hydroxymethylbenzofuran-5-yl)quinoline
https://huagongshe.com/reaction/2258515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 7-Chloro-2-(2-methoxycarbonylbenzofuran-5-yl)quinoline | HCID 22922182 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Chloro-2-(2-hydroxymethylbenzofuran-5-yl)quinoline | HCID 22922214 | — |
Reaction Steps
To a mixture of 7-chloro-2-(2-methoxycarbonylbenzofuran-5-yl)quinoline (0.92 g) in tetrahydrofuran (10 ml), lithium aluminum hydride (76.7 mg) was added dropwise under ice cooling. After being stirred for 2 hours, the resulting mixture was poured into a mixture of ice and diluted aqueous hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel and eluted with a mixture of ethyl acetate and toluene. The fractions containing object compound were combined, concentrated under reduced pressure, and recrystallized from toluene to give 7-chloro-2-(2-hydroxymethylbenzofuran-5-yl)quinoline (0.58
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05661159 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-988932bb048d42f0970fe16d23392df4 |
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| Source note | uspto-grants-1997_08 |
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