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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099016Generated: October 30, 2026

2-Fluoroethyl bromide → 1-(2-Fluoroethyl)-1,2,3,4-tetrahydro-7-quinolinol

https://huagongshe.com/reaction/2099016

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoroethyl bromideHCID 12982—
ReactantDiisopropylethylamineHCID 81531—
Reactant7-Quinolinol, 1,2,3,4-tetrahydro-HCID 93980—
SolventDimethylformamideHCID 6228—
Product1-(2-Fluoroethyl)-1,2,3,4-tetrahydro-7-quinolinolHCID 8586347344%

Reaction Steps

500 mg (3.35 mmol) 1,2,3,4-Tetrahydro-quinolin-7-ol are dissolved in 8 mL DMF and stirred at 60° C. overnight with 0.325 mL (1.3 eq) 1-bromo-2-fluoroethane, in the presence of 0.63 mL (1.1 eq) diisopropylethylamine. The reaction mixture is extracted with 0.1 N aqu. HCl and ethyl acetate. The combined organic extracts are washed with brine, dried over sodium acetate and evaporated. The residue is column chromatographed (silica gel, ethyl acetate/petroleum ether 1:2 to 1:1) to yield 290 mg (44%) desired product as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569337B2
Source datasetuspto-grants-2009_08
ORD IDord-ea436ee646474ad3b1fcd5f35788c6be
Source noteuspto-grants-2009_08