Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187282Generated: October 31, 2026

Sodium Hydroxide → 4-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1187282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
Reactant1-tert-Butyl-4-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrileHCID 45588333—
SolventSulfuric AcidHCID 1118—
Product4-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridineHCID 2351511550%

Reaction Conditions

Temperature120 °C

Reaction Steps

1-tert-Butyl-4-trifluoromethyl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile (25, 1.071 g, 4.007 mmol) is dissolved in 10 mL of aqueous 60% sulfuric acid and stirred at 120° C. for 20 hours. The reaction is adjusted to pH ˜7 with sodium hydroxide and aqueous saturated sodium bicarbonate, then extracted with ethyl acetate. The organic layer is washed with water, then brine and dried with magnesium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material is purified by silica gel column chromatography, eluting with ethyl acetate and hexane. Appropriate fractions are combined and concentrated under vacuum to provide the desired compound (26, 373 mg). MS (ESI) [M+H+]+=187.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673928B2
Source datasetuspto-grants-2014_03
ORD IDord-f15cf2b1a33445febdad509ab11cf864
Source noteuspto-grants-2014_03