HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179832Generated: October 30, 2026
Methyl Isobutyl Ketone → HCID 131733079, compound
https://huagongshe.com/reaction/2179832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Lithium bis((trifluoromethyl)sulfonyl)azanide | HCID 3816071 | — |
| Reactant | HCID 86658629 | HCID 86658629 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131733079 | HCID 131733079 | 87% |
Reaction Steps
A mixture of 2.87 g (3 mmol) of 3-butyl-2-(2-{3-[2-(3-butyl-1,1-dimethyl-1H-benzo[e]indol-2(3H)-ylidene)-ethylidene]-2-(phenylsulfonyl)cyclopent-1-en-1-yl}ethenyl)-1,1-dimethyl-1H-benzo[e]indol-3-ium p-toluenesulfonate, 1.31 g (4.5 mmol) of lithium bis(trifluoromethanesulfonyl)imide, 40 g of water, and 40 g of methyl isobutyl ketone was stirred for 8 hours at room temperature, whereupon the organic layer was taken out. The organic layer was combined with 0.43 g (1.5 mmol) of lithium bis(trifluoromethanesulfonyl)imide and 40 g of water and stirred overnight, whereupon the organic layer was taken out. The organic layer was washed with water and concentrated in vacuum. Diisopropyl ether was added to the residue for recrystallization. The crystal was collected and dried in vacuum, obtaining the target compound, 3-butyl-2-(2-{3-[2-(3-butyl-1,1-dimethyl-1H-benzo[e]indol-2(3H)-ylidene)ethylidene]-2-(phenylsulfonyl)cyclopent-1-en-1-yl}ethenyl)-1,1-dimethyl-1H-benzo[e]indol-3-ium bis(trifluoromethylsulfonyl)imide. Brown crystal, 2.9 g, yield 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09069245B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-152be1b6d37247bc9cfc3619f60a256d |
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| Source note | uspto-grants-2015_06 |
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