Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409710Generated: October 25, 2026

4-Amino-3-fluorophenol → HCID 67253219, compound

https://huagongshe.com/reaction/409710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3-fluorophenolHCID 2735919—
Reactanttert-Butyl 4-chloropicolinateHCID 11806045—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthyl AcetateHCID 8857—
ProductHCID 67253219HCID 6725321920%

Reaction Steps

Potassium tert-butoxide (5 g, 23.47 mmol, 1.4 eq) was dissolved in N,N-dimethylacetylamide (DMA, 12 mL). A solution of 3-fluoro-4-aminophenol (4.2 g, 32.86 mmol, 1.4 eq) in DMA (15 mL) was slowly added dropwise at 0° C. After the addition, the mixture was stirred at room temperature for 30 min. The mixture was heated to 100° C. and a solution of tert-butyl 4-chloropicolinate in DMA (18 mL) was slowly added dropwise, and then the mixture was stirred for 1 h. After being cooled to room temperature, ethyl acetate (500 mL) was added, and the resulted mixture was filtered to remove the undissolved material. The filtrate was washed with saturated brine (200 mL×3), dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to give a brown solid. The crude was purified by column chromatography (petroleum ether: ethyl acetate=3:1) to give the title compound (1.38 g, purity 98%, yield 20%) as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759531B2
Source datasetuspto-grants-2014_06
ORD IDord-993a73c0e6f046bd853091fd2b93e9d4
Source noteuspto-grants-2014_06