Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215802Generated: October 25, 2026

Sodium Bicarbonate → (7-Fluoro-2-methoxy-quinolin-8-yl)-methanol

https://huagongshe.com/reaction/215802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant8-(Bromomethyl)-7-fluoro-2-(methyloxy)quinolineHCID 66737650—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(7-Fluoro-2-methoxy-quinolin-8-yl)-methanolHCID 6673765573.2%

Reaction Steps

A suspension of 8-bromomethyl-7-fluoro-2-methoxy-quinoline (25 g, 92.56 mmol) in acetone (360 mL) and water (460 mL) was treated with NaHCO3 (12.74 g, 151.64 mmol, 1.6 eq.). The mixture was heated to reflux overnight. After cooling, the volatiles were removed in vacuo and the residue was partitioned between EA (300 mL) and water (100 mL). The aq. layer was extracted once with EA (250 mL) and the combined org. layers were washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by CC (Hept-EA 3:1) to afford the title alcohol as a yellowish solid (14.04 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193179B2
Source datasetuspto-grants-2012_06
ORD IDord-14de19d544bc4822b065ea209f0a6539
Source noteuspto-grants-2012_06