Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tetrabutylammonium | HCID 16028 | — |
| Reactant | alpha-Hydroxyacetophenone | HCID 68490 | — |
| Reactant | 3-Chloropropyl p-toluenesulfonate | HCID 69434 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 23036317 | HCID 23036317 | — |
Reaction Steps
2 ml of 2-hydroxy-acetophenone were added with stirring to a mixture of 2.31 g of tetrabutylammonium acid sulfate, 20 ml of 50% sodium hydroxide solution, 40 ml of benzene and 20 ml of acetonitrile and after adding 8.26 of 3-chloro-propyl p-toluene sulfonate, the mixture was heated under an inert atmosphere at 80° C. for 17 hours. The decanted aqueous phase was extracted with benzene and the organic phase was washed with water, dried over a deshydrant, filtered and evaporated to dryness. The residue was chromatographed over silica and eluted with a 95-5 benzene-ethyl acetate mixture. Evaporation ofthe solvents yielded 3.38 g of 1-[2-{3-chloropropoxy}-phenyl]-ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853408 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-dd604f2bf168483bad14b841bf70882c |
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| Source note | uspto-grants-1989_08 |
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