Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618897Generated: October 26, 2026

Hydrochloric Acid → (2-t-Butyl-phenyl)-(8-fluoro-quinolin-3-yl)-methanol

https://huagongshe.com/reaction/1618897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-tert-ButylbenzaldehydeHCID 13184777—
Reactant8-Fluoro-3-iodoquinolineHCID 16223764—
ReactantHCID 178418265HCID 178418265—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2-t-Butyl-phenyl)-(8-fluoro-quinolin-3-yl)-methanolHCID 6828942358.9%

Reaction Steps

After 3 ml of tetrahydrofuran was cooled to −10° C., 0.91 ml of n-butyllithium (2.6 M hexane solution) and 1.35 ml of n-butylmagnesium chloride (0.91 M tetrahydrofuran solution) were added. After 30 minutes of stirring, 0.98 g of 8-fluoro-3-iodoquinoline was added and the mixture was stirred for 15 minutes. 0.49 g of 2-t-butylbenzaldehyde was added to the reaction solution and the mixture was stirred for 3 hours. After dilute hydrochloric acid was added to the reaction mixture, the liquid was separated with ethyl acetate. After the organic layer was concentrated and purified by silica gel column chromatography, 0.55 g of (2-t-butyl-phenyl)-(8-fluoro-quinolin-3-yl)-methanol (Compound Number 54) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772200B2
Source datasetuspto-grants-2014_07
ORD IDord-6121e30fa300498ebc8e9c6f737901fe
Source noteuspto-grants-2014_07