Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Chloromethyl)quinoline | HCID 20394 | — |
| Reactant | 6-Hydroxy-chroman-4-one | HCID 7098944 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane ethylacetate | HCID 21226138 | — |
| Product | HCID 14422686 | HCID 14422686 | — |
Reaction Steps
A mixture of 6-hydroxy-4-chromanone (10.0 g, 0.0609 mol), 2-chloromethylquinoline (11.9 g, 0.0670 mol), sodium iodide (10.0 g, 0.0670 mol), potassium carbonate (25.3 g, 0.183 mol), and acetone (200 ml) was refluxed overnight under N2 atmosphere. After 17 hours the reaction appeared lighter and tlc analysis (10% EtOAc/CH2Cl2) indicated complete conversion of starting material to a slightly less polar product. The mixture was cooled, filtered, and the filtrate concentrated in vacuo. The residue was taken up in ethyl acetate (400 ml), washed with H2O and brine, dried over MgSO4, and concentrated in vacuo to a dark brown oil. Purification on a silica gel column eluted with 10% ethyl acetate/CH2Cl2 gave title product as an off-white solid, 15.3 g (82%), m.p. 112°-114° C.; tlc (1:9 ethyl acetate:CH2Cl2) Rf 0.30.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05059609 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-6514490ed9fd496fb688adeef1e4a7a7 |
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| Source note | uspto-grants-1991_10 |
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