Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 54486942 | HCID 54486942 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54468234 | HCID 54468234 | 95.3% |
Reaction Steps
33.4 g (0.093 mol) of N-[3-(4-bromophenyl)-prop-2-enyloxy]-phthalimide wereintroduced a little at a time into 50 ml of ethanolamine and the temperature increased to 30° C. during this procedure. The mixture was stirred for two hours at 60° C. and then allowed to cool, and 200 ml of dichloromethane were added. The mixture was extracted by shakingwith ice water. After drying was evaporating down the organic phase, the residue was recrystallized from petroleum ether. Yield: 95.3%; mp.: 35°-38° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05491123 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-952411edba40452cbd9dfbb28685eaa8 |
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| Source note | uspto-grants-1996_02 |
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