HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899967Generated: November 3, 2026
Water → 4-Hydroxymethyl-6-methoxyquinoline
https://huagongshe.com/reaction/899967
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl 6-methoxyquinoline-4-carboxylate | HCID 219907 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxymethyl-6-methoxyquinoline | HCID 338500 | 26.3% |
Reaction Steps
17 ml of a 1M solution of LiAlH4 in THF are added dropwise to a solution of 4 g of 4-ethoxycarbonyl-6-methoxyquinoline in 100 ml of anhydrous THF, under an inert atmosphere of argon at a temperature in the region of 5° C. The reaction medium is maintained with stirring for 16 hours at a temperature in the region of 20° C. 50 ml of water and 50 ml of ethyl acetate are added. After separation of the phases by settling, the organic phase is dried over sodium sulfate, filtered and then concentrated under reduced pressure. The foam obtained is purified by flash chromatography (SiO2, EtOAc as eluent, Ar). The fractions containing the product are concentrated under reduced pressure. 0.86 g of 4-hydroxymethyl-6-methoxyquinoline is thus obtained, the characteristics of which product are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354933B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-647272b0cf1d4b0a9fd9d4a82171054f |
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| Source note | uspto-grants-2008_04 |
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