HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 3-n-Butyl-5-(thiophen-2-yl methylene) hydantoin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | 3-Butylimidazolidine-2,4-dione | HCID 568235 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 3-n-Butyl-5-(thiophen-2-yl methylene) hydantoin | HCID 54116700 | 51.1% |
Reaction Steps
A mixture of thiophene-2-carboxaldehyde (5.6 g; 0.05 mole), 3-n-butylhydantoin (7.8 g; 0.05 mole) and ethanolamine (4.6 g; 0.075 mole) in water/ethanol (50 ml/30 ml) was stirred and boiled under reflux for 4 hours. The mixture was cooled in the refrigerator and the resultant brownish yellow crystals filtered off, washed with water, sucked dry and recrystallised from ethyl acetate (with carbon treatment) to give the title compound (6.4 g; 51%) having m.p. 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04293563 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-6702625bc23d4655ae427b9f26a2a1c2 |
| Source note | uspto-grants-1981_10 |