HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736679Generated: October 29, 2026
Methyl 4-Formylbenzoate → HCID 22282641, compound
https://huagongshe.com/reaction/736679
Participants
| Role | Name | HCID | Charge |
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| 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% |
Reaction Steps
4-Bromo-2-methylquinoline from (4a) (1.0 g, 4.5 mmol) was dissolved in 10 mL of anhydrous THF and the resulting solution was cooled to -78° C. A solution of n-BuLi (3.0 mL, 1.6 M, 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 and quenched with MeOH. The solution was 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 | US07595317B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-fb2fed4fa08d4bd29d54077a64b0ac0f |
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| Source note | uspto-grants-2009_09 |
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