HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680122Generated: November 1, 2026
Ammonia → 2-Amino-2,4-dimethylpentanenitrile
https://huagongshe.com/reaction/1680122
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2-Hydroxy-2,4-dimethylpentanenitrile | HCID 107230 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-2,4-dimethylpentanenitrile | HCID 92251 | — |
Reaction Steps
To a 1-liter autoclave were added 7 moles of ammonia and then 3.5 moles of 90%-pure 2-hydroxy-2,4-dimethylpentanonitrile, and the mixture was reacted at 27° C. for 10 hours at a rate of 300 r.p.m. Thus, 2-amino-2,4-dimethylpentanonitrile was synthesized. After reaction, the reaction mixture was taken out of the autoclave, and 44 g of the water phase was separated. The residue was distilled in a wetted wall tower under the following conditions: Temperature of the heating portion 25° C.; pressure 30 mmHg; and residence time in the heating portion 1 minute or less. Low-boiling compounds were thus distilled off and purified 2-amino-2,4-dimethylpentanonitrile was withdrawn from the bottom. The yield of the purified product was 90.0 mole % based on cyanohydrin. This purified product contained 0.5% by weight of ammonia and 0.8% by weight of hydrogen cyanide, and its purity was 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04272435 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-b8876ba487894cda80e0fd7f7c84600d |
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| Source note | uspto-grants-1981_06 |
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