HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029814Generated: October 26, 2026
Hydrogen Cyanide → 2-Amino-3-phenylpropanenitrile
https://huagongshe.com/reaction/1029814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Cyanide | HCID 768 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-3-phenylpropanenitrile | HCID 561384 | 70% |
Reaction Steps
1 millimole (0.117 g ) of benzyl cyanide is dissolved in 1 ml of anhydrous toluene at 0° C., under an argon atmosphere. 1.5 millimoles of a toluenic solution 1.5M of diisobutylaluminum hydride (1 m) are added dropwise at this temperature. The reaction mixture is maintained at 0° C. for 1 hour, then a solution of hydrocyanic acid (in excess) in tetrahydrofuran is added to this mixture, which is then maintained at room temperature for 3 hours, then hydrolyzed with 4 ml of methanol and pasty sodium sulfate. After an acid-base extraction, there are obtained 0.107 g of 2-amino-3-phenyl-propionitrile, in the form of a pale-yellow oil, with a yield of 70%,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05103019 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-e2bb83afbe5349f5ac7cf09efa963487 |
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| Source note | uspto-grants-1992_04 |
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