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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-indole-6-carbonitrile | HCID 85146 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indole-6-carbonitrile | HCID 86701728 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056874B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-294edd161127410d86008863fae613a8 |
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| Source note | uspto-grants-2015_06 |
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