HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095503Generated: October 25, 2026
Sodium Carbonate → 3-Methyl-2-trimethylsilanyl-1H-indole-5-carbonitrile
https://huagongshe.com/reaction/1095503
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(Trimethylsilyl)prop-1-yne | HCID 80363 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 4-Amino-3-iodobenzonitrile | HCID 4416395 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Methyl-2-trimethylsilanyl-1H-indole-5-carbonitrile | HCID 57475127 | — |
Reaction Steps
1-(Trimethylsilyl)propyne (2.23 ml, 1.68 g, 15.0 mmol), 4-amino-3-iodobenzonitrile (3.33 g, 13.65 mmol), lithium chloride (606 mg, 14.3 mmol) and sodium carbonate (4.35 g, 40.95 mmol) were added successively to abs. dimethylformamide (60 ml) under argon. Pd(dppf)Cl2 (1.116 g, 1.365 mmol) was added to this mixture and the reaction mixture was heated at 100° C. with exclusion of moisture for 6 h and then stirred at room temperature for 16 h. For working up of the mixture, water (150 ml) and ethyl acetate (300 ml) was added and the mixture was stirred for 10 min. After separation of the phases, the aqueous phase was extracted with ethyl acetate (3×100 ml). The combined organic phases were washed with saturated sodium chloride solution (3×100 ml), dried and concentrated. The residue was a brown oil (5.5 g) which, apart from 3-methyl-2-trimethylsilanyl-1H-indole-5-carbonitrile, contained traces of the isomer 2-methyl-3-trimethylsilanyl-1H-indole-5-carbonitrile and DMF.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138187B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-64a63c0078ea43af89051c3d46847bfe |
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| Source note | uspto-grants-2012_03 |
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