HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480123Generated: October 25, 2026
Ammonia → 2-Amino-3-cyclopropyl-2-methyl-propionitrile
https://huagongshe.com/reaction/1480123
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Cyclopropylpropan-2-one | HCID 537025 | — |
| Product | 2-Amino-3-cyclopropyl-2-methyl-propionitrile | HCID 84716049 | 177.2% |
Reaction Steps
To a round bottom flask equipped with a condenser was added magnesium sulfate (4.33 g, 35.9 mmol), sodium cyanide (3.52 g, 71.9 mmol) and ammonium chloride (1.92 g, 35.9 mmol). The solids were slurried in a 7.0M solution of ammonia in methanol (30.8 ml, 216 mmol) at room temperature. To the resulting suspension was added 1-cyclopropylpropan-2-one (CAN 4160-75-2, 8.3 g, 71.9 mmol) in one portion. The reaction mixture was stirred at room temperature for 4 hours. The solvents were removed under reduced pressure. The resulting slurry of the inorganic salts and product were diluted with tert-butylmethylether and solvent removed at reduced pressure. This process was repeated three times before the resulting suspension was filtered to remove the inorganic salts. The filtrate was then evaporated down to dryness to yield the crude product (7.9 g, 89%) as a yellow oil. MS (ESI, m/z): 125.3 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409866B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-cbce99c91cb54737a1dfdb27616d092c |
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| Source note | uspto-grants-2016_08 |
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