HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dihydroxybenzaldehyde → 1-[[(3,4-Dihydroxyphenyl)methylene]amino]-2-imidazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Amino-2-imidazolidinone hydrochloride | HCID 19261678 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[[(3,4-Dihydroxyphenyl)methylene]amino]-2-imidazolidinone | HCID 136081430 | — |
Reaction Steps
To a solution of 61.4 g (0.446 mol) of 1-amino-2-imidazolidinone hydrochloride in 300 ml of 80% aqueous ethanol were added 223 ml of 2N sodium hydroxide (0.446 mol) and a solution of 61.6 g (0.446 mol) of 3,4-dihydroxybenzaldehyde in 300 ml of 80% aqueous ethanol. The mixture was stirred for 20 minutes at room temperature, and the precipitate filtered off by suction, washed with ethanol and dried in vacuo (yield: 34.5 g; melting point 257° C., dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04801705 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-6457a2722da64e9a9deeb498ccf0a0dc |
| Source note | uspto-grants-1989_01 |