Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diphenylacetonitrile | HCID 6837 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12356700 | HCID 12356700 | — |
Reaction Steps
To a solution of diphenylacetonitrile (28 g) in ethanol (100 ml) were added DBU (6 ml) and ethyl acrylate (30 ml), and the mixture was heated and stirred at 80° C. for 16 hours. After cooling, 2N-hydrochloric acid (200 ml) was added and the mixture was extracted with isopropyl ether. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The crude crystal crop was recrystallized from hexaneisopropyl ether to provide the title compound (34 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05633248 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-45500bc5d2b740f7ad9d689e7536b18c |
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| Source note | uspto-grants-1997_05 |
|---|