HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966431Generated: October 25, 2026
Potassium Cyanide → 3-Methyl-2-(methylamino)-3-phenylbutanenitrile
https://huagongshe.com/reaction/966431
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 2-Methyl-2-phenylpropanal | HCID 283879 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Methyl-2-(methylamino)-3-phenylbutanenitrile | HCID 11708193 | 95% |
Reaction Steps
To a solution of potassium cyanide (103 g, 1.56 mol) and methylamine hydrochloride (106 g, 1.56 mol) in water (1000 mL) is added a solution of 2-methyl-2-phenylpropanal (222 g, 1.50 mol) in methanol (1000 mL) over a period of 30 minutes. An ice-water bath is used occasionally to maintain the reaction temperature between 20-25° C. The mixture is stirred at room temperature for 25 hours. Water (2000 mL) is then added and the reaction mixture is extracted with CH2Cl2 (3×800 mL). The combined organic extracts are washed with brine (500 mL) and dried over Na2SO4. The organic extracts are filtered and concentrated to give 3-methyl-2-(methylamino)-3-phenylbutanenitrile as an oil (274 g, 95% yield, 76.6% by HPLC area, NMR (>95%)). Evidence of decomposition on the HPLC/GC column is noted.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951955B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-229183f5043d4bfca086d132b31a2fc5 |
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| Source note | uspto-grants-2005_10 |
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