HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478284Generated: October 30, 2026
3-Aminocyclohex-2-en-1-one → HCID 10223145, compound
https://huagongshe.com/reaction/478284
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminocyclohex-2-en-1-one | HCID 78892 | — |
| Reactant | 3-Bromo-4-fluorobenzaldehyde | HCID 173604 | — |
| Reactant | 2H-Thiopyran-3,5(4H,6H)-dione | HCID 325286 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10223145 | HCID 10223145 | 31.8% |
Reaction Steps
A mixture of thiopyran-3,5-dione (Fehnel, E. A., J. Amer. Chem. Soc., (1955), 77, 4241-4244) (0.12 g, 1.0 mmol), 3-bromo-4-fluorobenzaldehyde (0.20 g, 1.0 mmol), 3-amino-2-cyclohexene-1-one (0.11 g, 1.0 mmol) and ethanol (5 mL) was heated to 80° C. in a sealed tube for 60 hours and cooled to ambient temperature. The resulting solid was collected by filtration, washed with ethanol and dried for 16 hours under high vacuum to provide the title compound (0.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642222B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-c11fe58ca9f342f7a890d8761fafbaa1 |
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| Source note | uspto-grants-2003_11 |
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