HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757147Generated: October 30, 2026
Ethanol → 3′,4′-Dihydro-6′-methoxyspiro[imidazolidine-4,1′(2′H)-naphthalene]-2,5-dione
https://huagongshe.com/reaction/1757147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3′,4′-Dihydro-6′-methoxyspiro[imidazolidine-4,1′(2′H)-naphthalene]-2,5-dione | HCID 2998139 | — |
Reaction Steps
A mixture of 35.2 g (0.2 mol) of 6-methoxy-1-tetralone, 19.5 g (0.3 mol) of potassium cyanide and 134.4 g (1.4 mol) of ammonium carbonate in 280 mL of EtOH was placed in a stainless steel bomb and heated at 110° C. for 48 hours. After cooling, the mixture was poured in 1.4 L of water. It was allowed to sit at ambient temperature for 3 days. The precipitated solid was filtered and washed several times with water and dried to give 48.1 g of a brown solid: mp 218°-220° C. 1H-NMR (DMSO-d6)d10.75(s, 1H),8.45(s, 1H),6.96(d, 1H),6.79 (d, 1H), 6.70 (s, 1H), 3.72 (s, 3H), 2.73 (t, 2H), 1.70-2.20 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05444079 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-e9803c80fb424abdb5adb117e7dd26f2 |
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| Source note | uspto-grants-1995_08 |
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