HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954Generated: October 25, 2026
Dimethylformamide → 5-[N-(4-formylphenyl)-N-(4-tolyl)amino]acenaphthene
https://huagongshe.com/reaction/1954
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5-[N-(4-tolyl)-N-phenylamino]acenaphthene | HCID 19688913 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[N-(4-formylphenyl)-N-(4-tolyl)amino]acenaphthene | HCID 19688918 | 97.1% |
Reaction Steps
4.7 g (0.014 mol) of the above prepared 5-[N-(4-tolyl)-N-phenylamino]acenaphthene was dissolved in 30 ml of N,N-dimethylformamide, and 3.22 g (0.021 mol) of phosphorus oxychloride was dropwise added thereto at room temperature for 10 minutes. After the temperature was raised to 50° C., and the mixture was stirred for 14 hours. The reaction was determined to be finished when disappearance of 5-[N-(4-tolyl)-N-phenylamino]acenaphthene was identified. The reaction product was poured into an aqueous solution having 10 g (0.23 mol) of 93% sodium hydroxide dissolved in 250 ml of water. The resultant mixture was cooled to precipitate a crystal, which was then filtrated, washed with water and dried to obtain 4.94 g (yield: 97.1%) of 5-[N-(4-formylphenyl)-N-(4-tolyl)amino]acenaphthene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728500 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-20078ac392344345839361b7b292e056 |
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| Source note | uspto-grants-1998_03 |
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