HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274533Generated: October 30, 2026
3-Bromoquinoline → HCID 21459047, compound
https://huagongshe.com/reaction/274533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromoquinoline | HCID 21413 | — |
| Reactant | 4-(Benzyloxy)-3-methoxybenzaldehyde | HCID 75506 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21459047 | HCID 21459047 | — |
Reaction Steps
A solution of 25.0 g of 3-bromoquinoline is dissolved in 200 ml of dry ether and cooled to -60° . At this temperature there are added dropwise within 15 minutes 75.1 ml of a 1.6 molar solution of n-butyllithium, whereupon the mixture is stirred for 10 minutes. A solution of 26.5 g of vanillin benzyl ether in 250 ml of dry ether is added dropwise thereto at -60°, the mixture is subsequently stirred at room temperature for 3 hours, poured into about 1.5 1 of ice-water and extracted three times with 600 ml of ethyl acetate each time. The organic phase is washed with water, dried over sodium sulfate and evaporated. The resulting oil is chromatographed on 1 kg of silica gel with methylene chloride/ethyl acetate (1:1). The crystalline crude product obtained is recrystallized from ethyl acetate. There is obtained α[4-(benzyloxy)-3-methoxyphenyl]-3-quinolinemethanol in the form of colourless crystals of m.p. 124°-125°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389653 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-cee1aafb718f4efe802ea7de22234bd6 |
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| Source note | uspto-grants-1995_02 |
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