HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089678Generated: November 1, 2026
4-Aminobenzonitrile → 4-{[Cyano(2-fluoro-3-hydroxy-5-methoxyphenyl)methyl]amino}benzonitrile
https://huagongshe.com/reaction/2089678
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Fluoro-3-hydroxy-5-methoxybenzaldehyde | HCID 59495309 | — |
| Catalyst | Guanidine Hydrochloride | HCID 5742 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-{[Cyano(2-fluoro-3-hydroxy-5-methoxyphenyl)methyl]amino}benzonitrile | HCID 67469955 | 93.9% |
Reaction Steps
Under nitrogen atmosphere, a solution of 2-fluoro-3-hydroxy-5-methoxybenzaldehyde (17.01 g, 100 mmol), 4-aminobenzonitrile (11.81 g, 100 mmol), and guanidine hydrochloride (287 mg, 3 mmol) in methanol (85 mL) was stirred at 40° C. for 1.5 hours. Trimethylsilylcyanide (18.1 mL, 130 mmol) was then added dropwise thereto, and the resulting mixture was stirred at 40° C. for 22 hours. After cooling the mixture, under cooling at 15° C., 3% aqueous sodium hydrogen carbonate solution (87.65 g) was added dropwise thereto, and the resulting mixture was stirred for 1 hour under cooling at 10° C. The precipitated solid was filtered and dried to obtain the captioned compound (27.91 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436009B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-1b2f7d66405c4f43acc7030397091728 |
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| Source note | uspto-grants-2013_05 |
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