HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414075Generated: October 25, 2026
Ammonia → 2-(2-Diisopropylamino ethyl) 3,3-dimethyl 2-(2-pyridyl) pentane-dinitrile
https://huagongshe.com/reaction/2414075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 3-Methyl-2-butenenitrile | HCID 94301 | — |
| Reactant | 4-Diisopropylamino 2-(2-pyridyl)butyronitrile | HCID 13319674 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Diisopropylamino ethyl) 3,3-dimethyl 2-(2-pyridyl) pentane-dinitrile | HCID 54234562 | — |
Reaction Steps
The mixture of 4.7 g of sodium amide and 400 ml of liquid ammonia is cooled to -40° C., then the solution of 24.5 g of 4-diisopropylamino 2-(2-pyridyl) butane nitrile (Example 1a) in 30 ml of anhydrous ether is added, the temperature being maintained between -40° C. and -33° C. The mixture is stirred for 15 mins. at this temperature then the solution of 9 g of 3,3-dimethyl acrylonitrile in 40 ml of ether is added, still at the same temperature. The temperature is allowed to rise slowly up to ambient temperature (duration: about 5 hrs.). 200 ml of ether are added then water is added drop by drop. The ethereal phase is separated and the aqueous phase is re-extracted with ether. The ethereal extracts are collected and dried over sodium sulfate. The solvent is evaporated to dryness and the residue is chromatographed over a column of alumina with the eluting ethyl acetate-pentane (2.5-100) vol/vol mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04721710 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-b58ef02f0aaf4f5d8b614354929b82db |
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| Source note | uspto-grants-1988_01 |
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