Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 20095027 | HCID 20095027 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20095049 | HCID 20095049 | — |
Reaction Steps
Subsequently, 450 ml of dry dichloromethane and 68.7 g (5.15×10-1M) of anhydrous aluminum chloride were placed in a 1 liter-reaction vessel and cooled below 0° C. To the mixture, 37.2 g (4.74×10-1M) of acetyl chloride was added dropwise in 10 minutes below 0° C. and then 90 g (3.91×10-1M) of the above prepared 2-octylindan was added dropwise below 0° C., followed by stirring for 2 hours below 0° C. and further stirring for 2 hours at room temperature. After the reaction, the reaction mixture was poured into 1 liter of ice water and 90 ml of concentrated sulfuric acid was added. The dichloromethane layer was separated from the above mixture and washed with water, followed by drying with anhydrous magnesium sulfate and distilling-off of the solvent to obtain a crude product. The crude product was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=20/1) to obtain 57.6 g of 2-octyl-5-acetylindan.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05385692 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-d08fe370305149d5b76900ed33bcdfc1 |
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| Source note | uspto-grants-1995_01 |
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