Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | HCID 20095049 | HCID 20095049 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20095034 | HCID 20095034 | 77.3% |
Reaction Steps
In a 3 liter-reaction vessel, 50 g (1.84×10-1M) of the above-prepared 2-octyl-5-acetylindan and 500 ml of 1,4-dioxane were placed and warmed to 25° C. To the mixture, a mixture solution of 482 g of 10% -sodium hypochlorite aqueous solution and 178 g of 25%-sodium hydroxide aqueous solution was added dropwise in 30 minutes at about 30° C., followed by stirring for 6 hours at 60° C. After the reaction, the reaction mixture was cooled to 40° C. and then a solution of 22 g of sodium sulfite in 750 ml of water was added thereto, followed by stirring for 30 minutes. To the resultant mixture, 380 ml of concentrated sulfuric acid was added to precipitate a crystal. The crystal was recovered by filtration and washed with water, followed by drying and recrystallization from ethanol to obtain 37.0 g of 2-octylindan-5-carboxylic acid.
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-5e29a8f5defc40f2b907bf9f71d6258f |
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| Source note | uspto-grants-1995_01 |
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