Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 2-Imidazolidinone | HCID 8453 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 19261677 | HCID 19261677 | 87% |
Reaction Steps
A stirring solution of 65 g (0.75 mole) of 2-imidazolidinone in 2000 ml of 2 N H2SO4 is cooled to SAC. A 53 g (0.77 mole) portion of NaNO2 is added portionwise, over a 15 minute period, maintaining the temperature at 0° C. The resulting mixture is stirred at 0° C. for 2 hours. A 108 g (1.65 mole) portion of zinc dust is added portionwise, over a 1 hour period, maintaining the temperature at 0° C. The reaction is stirred at 0° C. for 0.5 hour and then at ambient temperature for 1 hour. The excess zinc is removed by filtration. The filtrate is treated all at once, with a solution of 80 g (0.75 mole) of benzaldehyde, in 400 ml of S.D.A. #32 and the resulting mixture is stirred for 16 to 18 hours at ambient temperature. The solid is collected by filtration, washed with H2O, and air-dried to yield 124 g (87%) of 1-[(phenylmethylene)amino]-2-imidazolidinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06083945 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-bb4f1fc7dcff4a5bb4d3b3addcdbe99c |
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| Source note | uspto-grants-2000_07 |
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