HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608561Generated: October 31, 2026
HCID 86751038, compound → HCID 86748545, compound
https://huagongshe.com/reaction/1608561
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86751038 | HCID 86751038 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86748545 | HCID 86748545 | 91.3% |
Reaction Steps
A solution of the N-aryl lactam XIV (4.88 g, 16.2 mmol) was dissolved in acetonitrile (50 mL) and cooled to 0°-5° C. in an ice bath. To this was added a cold solution of ceric ammonium nitrate (26.6 g, 48.6 mmol, 50 mL) in one portion. The deep red reaction was allowed to stir for 10 min and during that time the color gradually lightened to orange. The cold solution was transferred to a separatory funnel, diluted with water, and extracted with ethyl acetate. The organic fraction was washed with several portions of 10% aqueous sodium sulfite, followed by saturated aqueous sodium bicarbonate. The organic fraction was dried (MgSO4) and concentrated to give the desired product (2.71 g, 91%) as a yellow-orange solid that was used directly in the next step; 1H NMR (300 MHz, CDCl3): δ 6.11 (bs, 1H), 5.73 (dd, 1H, J=2.2, 4.7 Hz), 5.12-5.08 (m, 1H), 4.63 (dd, 1H, 4.7, 9.1 Hz), 2.09 (s, 3H), 1.75 (s, 3H), 1.67 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05395850 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-ce9dc270696f4a59a7b22413fdf30e5c |
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| Source note | uspto-grants-1995_03 |
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