HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198935Generated: October 31, 2026
N-[4-(2,2-Dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)phenyl]-N-methylformamide → 4-(2,2-Dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N-methylaniline
https://huagongshe.com/reaction/2198935
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-[4-(2,2-Dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)phenyl]-N-methylformamide | HCID 3061435 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2,2-Dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N-methylaniline | HCID 3061434 | 55% |
Reaction Steps
5 g of 4'-(2,2-dimethyl-4-phenyl-3-oxazoline-5-yl)-N-methylformanilide were exposed to light in 2 liters of ethanol under an atmosphere of argon for 8 hours in the apparatus described in Example 4. After evaporation of the solvent in a water-jet vacuum, there remained behind an oil which was chromatographed on silica gel. The elution was carried out with dichloromethane/acetone (95:5). In order to remove accompanying impurities, the product isolated in the foregoing manner was suspended in hot petroleum ether (boiling range 80°-110° C.), removed by filtration under suction and washed on the suction filter with petroleum ether. After drying at 60° C. in a water-jet vacuum, there were obtained 2.5 g of 5-[p-(methylamino)phenyl]-2,2-dimethyl-4-phenyl-3-oxazoline having a melting point of 138°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04360530 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-19319f3963214018ac2c5bb1d375b25f |
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| Source note | uspto-grants-1982_11 |
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