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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40316Generated: October 26, 2026

2-(Quinolin-6-yl)propanoic acid → 2-Fluoro-2-(quinolin-6-yl)propanoic acid

https://huagongshe.com/reaction/40316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Quinolin-6-yl)propanoic acidHCID 19036006—
ReactantMethyl 2-fluoro-2-(quinolin-6-yl)propanoateHCID 67503402—
Product2-Fluoro-2-(quinolin-6-yl)propanoic acidHCID 57691062—

Reaction Steps

To a solution of methyl 2-(quinolin-6-yl)propanoate (0.868 g, 4.03 mmol) in THF (1.1M, 3.7 mL) at −78° C. was added LiHMDS (1M in THF) (5.24 ml, 5.24 mmol). The reaction was stirred at −78° C. for ˜15 minutes, then to it was added a solution of N-fluorobenzenesulfonimide (1.40 g, 4.44 mmol) in THF (1.0M, 4.5 mL). The reaction was allowed to warm to −10° C. over 2 h. The reaction was filtered through a plug of Celite, washed with EtOAc and the filtrate was then concentrated in vacuo. The concentrated material was rediluted with EtOAc and washed with saturated NH4Cl solution. The aqueous layer was then extracted with EtOAc, and the organic layers were dried over MgSO4, filtered and concentrated in vacuo. The crude material was dissolved in minimal DCM and purified via MPLC (eluting with isocratic 40% EtOAc:Hexanes to yield methyl 2-fluoro-2-(quinolin-6-yl)propanoate (0.709 g, 75.4% yield) as a yellow oil. To synthesize the corresponding acid, methyl 2-fluoro-2-(quinolin-6-yl)propanoate was saponified in a method similar to that of 2-(quinolin-6-yl)propanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524900B2
Source datasetuspto-grants-2013_09
ORD IDord-82114ff7e3584801b7f5753c8f1a9749
Source noteuspto-grants-2013_09