Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12811402 | HCID 12811402 | — |
| Reactant | HCID 86739088 | HCID 86739088 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 20484445 | HCID 20484445 | — |
Reaction Steps
Potassium iodide (0.075 g) was added to a stirred solution of chloroacetone (3 ml) in dry acetone (3.5 ml) and the mixture was stirred for 16 hours. 2-Methoxy-5-methyl-4-methylsulphinylphenol (5.0 g) and potassium carbonate (0.85 g) were heated at reflux with stirring in dry acetone (25 ml). The chloroacetone/potassium iodide solution and potassium carbonate (3.4 g) were then added in four equal portions over 2 hours. The mixture was heated at reflux for a further 2 hours, cooled and filtered, the filter cake being washed well with acetone. The acetone was removed under reduced pressure and the residue chromatographed on a column of silica gel eluting with methylene chloride/methanol mixtures (gradient I to 3% v/v methanol). Trituration with diethyl ether gave the ketone (4.6 g) as colourless crystals, m.p. 104°-106°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04410548 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-63efcc6a2b6b40e595d0c33c18d4cc64 |
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| Source note | uspto-grants-1983_10 |
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