Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-(4-ethoxyphenyl)acetyl Chloride | HCID 11629782 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Ethoxy-2-tetralone | HCID 4694031 | — |
Reaction Steps
39.1 g (0.20 mol) of 4-ethoxyphenylacetyl chloride in 200 ml of dichloromethane were added dropwise in the course of 1 hour at −78° C. to 53.4 g (0.4 mol) of aluminum chloride in 800 ml of dichloromethane. A vigorous stream of ethylene was subsequently passed in in the course of 15 minutes, and the mixture was allowed to come to room temperature and stirred for a further 3 hours. The dark red solution was cooled to 0° C. and carefully treated with 300 ml of ice-water. After phase separation, the organic phase was washed with 2N HCl (3×) and saturated sodium hydrogen carbonate solution, dried and evaporated on a rotary evaporator. After purification by column chromatography with petroleum ether/ethyl acetate (9:1, 8:2), 20.9 g (56% of theory) of a yellow syrup were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265398B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-0fe0cdefbb12467cbe006d2f5dd21b98 |
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| Source note | uspto-grants-2001_07 |
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