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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624947Generated: October 30, 2026

Hydrochloric Acid → 5-Bromo-6-(2,2,3,3,3-pentafluoro-propoxy)-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/624947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2,3,3,3-PentafluoropropanolHCID 9872—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant5-Bromo-6-chloropicolinic acidHCID 44607714—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-6-(2,2,3,3,3-pentafluoro-propoxy)-pyridine-2-carboxylic acidHCID 8667478522%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 6-chloro-5-bromo-pyridine-2-carboxylic acid (CAN 959958-25-9, 1.7 g, 7.19 mmol) in DMF (90 mL) and THF (30 mL) was added potassium tert-butoxide (2.02 g, 18.0 mmol) and 2,2,3,3,3-pentafluoropropan-1-ol (5.73 mL, 57.5 mmol). The mixture was stirred at 140° C. for 4 days, cooled and poured into ice-water (100 mL). 2 M Hydrochloric acid (15 mL) was added to adjust the pH to 2-3 and the mixture was extracted with TBME, organic layers were washed twice with water, pooled, dried with Na2SO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, ethyl acetate/n-heptane gradient) to give the title compound (548 mg, 22%) as light-brown solid; LC-MS (UV peak area, ESI) 100%, 347.9306 [M−H−].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303012B2
Source datasetuspto-grants-2016_04
ORD IDord-d68ba1923fc0461798d28d9c00cef0c1
Source noteuspto-grants-2016_04