HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485115Generated: October 25, 2026
Ammonia → 2-Amino-2-(4-iodophenyl)acetonitrile
https://huagongshe.com/reaction/1485115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 4-Iodobenzaldehyde | HCID 96657 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Titanium isopropoxide | HCID 11026 | — |
| Product | 2-Amino-2-(4-iodophenyl)acetonitrile | HCID 67151559 | — |
Reaction Steps
To a solution of 4-iodobenzaldehyde (10.4 g) in methanol (36 mL), tetraisopropyl orthotitanate (50.0 mL) and a solution (50 mL) of 8 mol/L ammonia in methanol were added and the mixture was stirred at room temperature for 3.5 hours. Trimethylsilyl cyanide (5.89 mL) was slowly added to the mixture, which was then stirred at the same temperature for 14 hours. Iced water was added to the reaction mixture, which was then filtered through Celite (registered trademark). The filtrate was concentrated under reduced pressure and the resulting residue was extracted with ethyl acetate. The combined organic layers were washed with water and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=99:1-25:75) to give amino(4-iodophenyl)acetonitrile as a pale yellow solid (5.05 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422240B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-e3a69db3aa75466abea85074d02c8e6e |
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| Source note | uspto-grants-2016_08 |
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