Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 2-Methoxypropanenitrile | HCID 141829 | — |
| Reactant | HCID 13931490 | HCID 13931490 | — |
| Reactant | HCID 19915421 | HCID 19915421 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86745402 | HCID 86745402 | — |
Reaction Steps
As in Example 1, bis(2-cyanoethoxy)ethane was prepared by the addition of 623 g (11.73 moles) of acrylonitrile to 310 g (5.0 moles) of ethylene glycol containing 1.0 g of anhydrous lithium hydroxide at 55°-60° C. over a period of 90 min. The reaction was permitted to stir an additional 2 hr at 50° C. The reaction contents were cooled to 25° C. and 88.0 g (2.75 moles) of methanol was added over a period of 1 hr while maintaining the temperature between 25°-30° C. The mixture was allowed to stir an additional 12 hr at room temperature. Analysis by NMR revealed the crude product mixture to be 79.7 wt % of bis(2-cyanoethoxy)ethane, 17.4 wt % methoxypropionitrile, 1.78 wt % methanol, 0.72 wt % of 2-cyanoethoxyethanol, and 0.33 wt % acrylonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05081305 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-26b1c6a0de924aad998b2b0f5590e6c4 |
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| Source note | uspto-grants-1992_01 |
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