HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179831Generated: November 1, 2026
Methyl Isobutyl Ketone → HCID 87403260, compound
https://huagongshe.com/reaction/2179831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Potassium perfluorobutanesulfonate | HCID 23675274 | — |
| Reactant | HCID 86658629 | HCID 86658629 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 87403260 | HCID 87403260 | 92% |
Reaction Steps
A mixture of 0.96 g (1 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, 0.51 g (1.5 mmol) of potassium perfluorobutanesulfonate, 20 g of water, and 20 g of methyl isobutyl ketone was stirred for 6 hours at room temperature, whereupon the organic layer was taken out. The organic layer was combined with 0.17 g (0.5 mmol) of potassium perfluorobutanesulfonate and 20 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 perfluorobutanesulfonate. Brown crystal, 1.1 g, yield 92%.
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-655e5d9a15254debbae47c8a673c26a9 |
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| Source note | uspto-grants-2015_06 |
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