HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380141Generated: October 30, 2026
Water → 1-[8-(Benzyloxy)quinolin-5-yl]ethan-1-one
https://huagongshe.com/reaction/1380141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(8-Hydroxyquinolin-5-yl)ethan-1-one--hydrogen chloride (1/1) | HCID 20026880 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[8-(Benzyloxy)quinolin-5-yl]ethan-1-one | HCID 13744891 | 57.1% |
Reaction Steps
27 g of 5-acetyl-8-hydroxyquinoline hydrochloride are dissolved in 540 ml of anhydrous dimethylformamide and 50 g of powdered potassium carbonate are added thereto. 18.4 g of benzyl chloride are added to the mixture at 50° C. under an argon atmosphere, and the mixture is stirred at the same temperature for 4.5 hours and then further stirred at room temperature for 1.5 hours. After the reaction, water is added to the mixture, and the aqueous mixture is extracted with ethyl acetate. The extract is washed with water, a saturated sodium chloride solution, dried and then evaporated under reduced pressure to remove ethyl acetate. The residue is recrystallized from ethanol. 19.1 g of 5-acetyl-8-benzyloxyquinoline are obtained as brownish prisms. 6.35 g of said product are further recovered from the mother liquor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04579854 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-99211616f59f4803bbd98015a4ae2dfd |
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| Source note | uspto-grants-1986_04 |
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