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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258465Generated: October 27, 2026

Ethanol → 3-(7-Chloroquinol-2-ylmethoxy)benzyl alcohol

https://huagongshe.com/reaction/258465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant3-((7-Chloro-2-quinolinyl)methoxy)benzaldehydeHCID 19002899—
SolventTetrahydrofuranHCID 8028—
Product3-(7-Chloroquinol-2-ylmethoxy)benzyl alcoholHCID 19737240102%

Reaction Steps

The aldehyde of Step 1 (46.64 g, 156.6 mmol) was dissolved in 300 mL of THF. At 0° C., 800 mL of EtOH was added, followed by NaBH4 (5.93 g, 157 mmol). The mixture was then stirred at r.t. (room temperature) for 1 h and poured into cold 25% aq (aqueous) NH4OAc. The organic solvents were evaporated and the title alcohol was extracted with toluene:THF 1:1, dried over Na2SO4 and filtered through silica to yield 47.9 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266568
Source datasetuspto-grants-1993_11
ORD IDord-c1f2efb795f7473f9cc6fe029ed93581
Source noteuspto-grants-1993_11