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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384435Generated: October 31, 2026

Water → [4-(Benzyloxy)-8-methoxy-3-methylquinolin-2-yl]methanol

https://huagongshe.com/reaction/384435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium SulfateHCID 24436—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantEthyl 4-(benzyloxy)-8-methoxy-3-methylquinoline-2-carboxylateHCID 59527045—
SolventTolueneHCID 1140—
Product[4-(Benzyloxy)-8-methoxy-3-methylquinolin-2-yl]methanolHCID 5952684032.1%

Reaction Steps

To a solution of ethyl 4-(benzyloxy)-8-methoxy-3-methylquinoline-2-carboxylate (1.95 g) in toluene (30 mL) was added dropwise a solution of diisobutylaluminum hydride in toluene (0.99M, 6.1 mL) at room temperature under nitrogen flow, followed by stirring. After 1 hour and 2 hours, a solution of diisobutylaluminum hydride in toluene (0.99M, each 6.1 mL) was added thereto, followed by stirring for 3 hours. Water was added to the reaction mixture to stop the reaction, and then anhydrous sodium sulfate was added thereto, followed by stirring. Insolubles were removed by filtration through Celite. The filtrate was concentrated under reduced pressure, and then the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=50/50˜ethyl acetate, then chloroform˜chloroform/methanol=95/5) to obtain [4-(benzyloxy)-8-methoxy-3-methylquinolin-2-yl]methanol (551 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-30aad7794a8849cfb9112ce4d3c55cb9
Source noteuspto-grants-2013_02