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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490276Generated: October 29, 2026

Sodium Bicarbonate → 4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/490276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-Chloro-1-(4-methylbenzene-1-sulfonyl)-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridineHCID 11689317—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridineHCID 1162992174.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

52.3 g (200 mmol) of tetra-n-butylammonium fluoride are added to a solution of 30 g (80.0 mmol) of 4-chloro-1-(toluene-4-sulphonyl)-3-trifluoromethyl-1H-pyrrolo[2,3-b]pyridine in 250 ml of absolute THF and the mixture is stirred at 20° C. for 20 minutes. On completion of conversion (TLC monitoring), the mixture is admixed with 300 ml of saturated NaHCO3 solution and subsequently extracted three times with 500 ml each time of ethyl acetate. The combined organic phases are washed with saturated NaCl solution, dried over MgSO4 and freed of volatile constituents in a water-jet vacuum. Purification of the crystalline crude product by chromatography through silica gel (CH2Cl2: MeOH=30:1) results in 13.1 g (59.5 mmol; 74%) of 4-chloro-3-trifluoromethyl-1H-pyrrolo[2,3-b]pyridine as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528146B2
Source datasetuspto-grants-2009_05
ORD IDord-ba533b2943a644059e1d0cc260235337
Source noteuspto-grants-2009_05