Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3H-Indole, 2,3,3-trimethyl- | HCID 15427 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20080311 | HCID 20080311 | 82% |
Reaction Steps
To a solution of 1.6 g of 2,3,3-trimethylindolenine in 10 ml of chloroform was added 2.8 g of 1-bromododecane and the mixture was heated in an autoclave at 80° C. for 20 hours. The resulting precipitate was recovered by filtration to give 3.7 g of 1-dodecyl-2,3,3-trimethylindolenium as white crystals. To the crystals thus obtained was added 40 ml of 10N aqueous potassium hydroxide solution in a nitrogen atmosphere and the mixture was heated at 50° C. for 3 hours. The reaction mixture was then extracted with ether and the extract was dried over magnesium sulfate and concentrated under reduced pressure to give 2.7 g of 3,3-dimethyl-1-dodecyl-2-methyleneindoline (Yield 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403702 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-95a67b91c2af47ee82570e0321c5a8a7 |
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| Source note | uspto-grants-1995_04 |
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