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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420096Generated: October 27, 2026

4-Methoxybenzyl alcohol → 4-(4-methoxybenzyloxy)-2,8-dichloro-7-methoxyquinoline AI

https://huagongshe.com/reaction/420096

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant15-Crown-5HCID 36336—
Reactant2,4,8-Trichloro-7-methoxyquinolineHCID 2794516—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(4-methoxybenzyloxy)-2,8-dichloro-7-methoxyquinoline AIHCID 8663321056%

Reaction Steps

Sodium hydride (2.74 g, 1.2 eq.) was added portionwise to a solution of p-methoxybenzyl alcohol (8.55 mL, 1.2 eq.) and 15-crown-5 (13.6 mL, 1.2 eq.) in 35 mL of DMF. The mixture was allowed to stir at room temperature for 30 min, and then added to a solution of 2,4,8-trichloro-7-methoxyquinoline (15 g, 1 eq.) in DMF (75 mL) via canula. After 18 hrs of stirring at room temperature, the mixture was poured on 500 mL of water and NH4Cl aqueous. Ethyl acetate (200 mL) was added and the precipitate was filtered. The filtrate was purified by chromatography on silica gel to yield compound AI in 56% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093379B2
Source datasetuspto-grants-2012_01
ORD IDord-24325da4403c4308a791a31e313de483
Source noteuspto-grants-2012_01