Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromopropionitrile | HCID 17020 | — |
| Reactant | trans-2,6-Dimethylmorpholine | HCID 11137133 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 28372791 | HCID 28372791 | 79.3% |
Reaction Steps
3-Bromopropionitrile (4.06 g, 0.03 mole), cis/trans-2,6-dimethylmorpholine (4.0 g, 0.034 mole), triethylamine (5.0 ml ) and ethanol (50 ml ) were refluxed (78° C.) for 3 hours and left stirring at 20° C. for 17 hours. The solvent was evaporated and the residue purified by chromatography using silica gel/chloroform: 5% methanol to give els/trans N-(2-cyanoethyl)-2,6-dimethylmorpholine (4.0 g, 79%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05332753 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-062533deb8344ca9b9523766c1265bcf |
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| Source note | uspto-grants-1994_07 |
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