HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085350Generated: October 31, 2026
Methyl 4-Formylbenzoate → HCID 22282641, compound
https://huagongshe.com/reaction/2085350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | 4-Bromo-2-methylquinoline | HCID 15560677 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22282641 | HCID 22282641 | 65.1% |
Reaction Steps
4-Bromo-2-methylquinoline (53a) (1.0 g, 4.5 mmol) was dissolved in 10 mL of anhydrous THF and the resulting solution was cooled down to −78° C. A solution of n-BuLi (3.0 mL, 1.6M, 4.8 mmol) was added slowly and the resulting solution was maintained at −78° C. for 5 min. Meanwhile, in another flask methyl 4-formylbenzoate (0.9 g, 5.4 mmol) was dissolved in 20 mL of anhydrous THF and the resulting solution was cooled to −78° C. before the lithium reagent made above was cannulated. The whole mixture was stirred for 30 min before quenched with MeOH. The solution was then diluted with ethyl acetate and washed with H2O and brine. After dried over MgSO4, the organic solution was filtered and concentrated. The residue was purified on silica gel to provide methyl 4-[hydroxy(2-methyl-4-quinolinyl)methyl]benzoate (0.9 g, 65%). MS (AP+): 308 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06720329B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-b07389c26c4e4a808d47598e361f1fe4 |
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| Source note | uspto-grants-2004_04 |
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