HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161367Generated: October 29, 2026
4-Aminobenzonitrile → HCID 59517247, compound
https://huagongshe.com/reaction/1161367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Ytterbium triflate | HCID 2733225 | — |
| Reactant | HCID 13861691 | HCID 13861691 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59517247 | HCID 59517247 | — |
Reaction Steps
After adding 1.23 g of 4-aminobenzonitrile [CAS No. 873-74-5], 1.92 g of 2-fluoro-3,5-dimethoxybenzaldehyde [CAS No. 113984-71-7], 1.0 g of MS3A and 2.77 ml of trimethylsilyl cyanide to a solution of 0.645 g of Yb(OTf)3 in 20 ml of dichloromethane under a nitrogen atmosphere, the mixture was stirred at room temperature for 20 hours. After then adding 500 ml of ethyl acetate and 300 ml of water to the reaction mixture, it was filtered through celite and the celite was washed with 500 ml of ethyl acetate. The organic layers were combined and dried over anhydrous magnesium sulfate. The desiccating agent was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (2.59 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816522B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-6e4e2b7e5e234fcf8c7069384e061ad0 |
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| Source note | uspto-grants-2010_10 |
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