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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693696Generated: October 30, 2026

Sodium hydride → HCID 57537522, compound

https://huagongshe.com/reaction/1693696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTriisopropylsilyl chlorideHCID 139400—
Reactant4-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridineHCID 23515115—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57537522HCID 5753752291.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Trifluoromethyl-1H-pyrrolo[2,3-b]pyridine (1.5 g, 8 mmol) was suspended in tetrahydrofuran (20 mL) and cooled to 0° C. Sodium hydride (390 mg, 9.7 mmol) was added in small portions and the mixture was stirred at 0° C. for 1 h. Triisopropylsilyl chloride (2.6 mL, 12 mmol) was added and the mixture was stirred at 23° C. for 12 h. The reaction was quenched with saturated ammonium chloride solution (10 mL) and diluted with water (5 mL). The mixture was applied to a Varian chemelut cartridge and eluted with ethyl acetate. Purification by flash silica gel chromatography using a gradient of dichloromethane in hexanes afforded 4-Trifluoromethyl-1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine (2.5 g, 7.3 mmol, 90% yield). 1H NMR (500 MHz, DMSO-d6) δ 8.44 (d, J=5 Hz, 1H), 7.76 (d, J=4 Hz, 1H), 7.44 (d, J=5.5 Hz, 1H), 6.74 (m, 1H), 1.88 (septet, J=7.5 Hz, 3H), 1.05 (d, J=7.5 Hz, 18H). MS: m/z 343.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158647B2
Source datasetuspto-grants-2012_04
ORD IDord-625e60ed907d4cfc902b09cc14a3e7d2
Source noteuspto-grants-2012_04