HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369422Generated: October 27, 2026
4-Hydroxybenzaldehyde → 4-(2-quinolinylmethoxy)Benzaldehyde
https://huagongshe.com/reaction/369422
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Chloromethyl)quinoline hydrochloride | HCID 3083823 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-quinolinylmethoxy)Benzaldehyde | HCID 14578960 | 91% |
Reaction Steps
2-Chloromethylquinoline hydrochloride (6.42 g, 30 mmol), 4-hydroxybenzaldehyde (3.66 g, 30 mmol) and potassium carbonate (9.12 g, 66 mmol) were combined, to which 50 ml of DMF were added. The resulting mixture was stirred overnight at 90° C. The solvent was driven off under reduced pressure, the residue was extracted with ethyl acetate. The organic layer was washed with 1 N aqueous solution of sodium hydroxide and a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, whereby 7.19 g of the title compound were obtained (yield: 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136848 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-5f7fe61a123447d3aa0c0d1a7700f7ac |
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| Source note | uspto-grants-2000_10 |
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