Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Product | 4-Chloro-4'-methoxybutyrophenone | HCID 96414 | 97,802.898% |
Reaction Steps
To a cooled solution of 10.8 g (0.1 mol) anisole in 100 ml anhydrous toluene 13.3 g (0.1 mol) aluminium trichloride was added in portions over 15 minutes at −10° C. then 15.5 g (12.3 ml, 0.1 mmol) 4-chloro-butyryl chloride were added over 15 minutes keeping the temperature at −10° C. After stirring for additional 30 minutes at −10° C. the reaction mixture was hydrolyzed and the layers were separated. The aqueous layer was extracted with toluene (three times 100 ml) and the combined organic layers were dried and evaporated to yield 20.8 g (97%) 4-chloro-1-(4-methoxy-phenyl)-butan-1-one as a light beige liquid that solidified on standing. The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288557B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-b118ea003b0d422cbbcaa1deda55d693 |
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| Source note | uspto-grants-2007_10 |
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