Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174092Generated: October 31, 2026

Sodium hydride → 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indole-6-carbonitrile

https://huagongshe.com/reaction/2174092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1H-indole-6-carbonitrileHCID 85146—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
SolventDimethylformamideHCID 6228—
Product1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indole-6-carbonitrileHCID 86701728—

Reaction Conditions

Temperature0 °C

Reaction Steps

1H-Indole-6-carbonitrile (CAS #:15861-36-6) (1.47 g, 10.34 mmol) was dissolved in DMF (103 mL) and cooled to 0° C. NaH (60% in mineral oil, 0.620 g, 15.51 mmol) was added in one batch. The reaction was allowed to stir at room temperature for 15 minutes. SEMCl (2.38 mL, 13.44 mmol) was added at 0° C. and stirred for 20 minutes. The reaction was quenched with saturated ammonium chloride and then EtOAc was added. The organic layer was removed and the water layer was extracted again with EtOAc. The combined organics were washed with water, dried over MgSO4 filtered and concentrated. The resulting residue was purified via flash chromatography (0-50% EtOAc:heptanes) to obtain title compound. MS (ESI+) m/z 273.23 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056874B2
Source datasetuspto-grants-2015_06
ORD IDord-294edd161127410d86008863fae613a8
Source noteuspto-grants-2015_06