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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179831Generated: November 1, 2026

Methyl Isobutyl Ketone → HCID 87403260, compound

https://huagongshe.com/reaction/2179831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Isobutyl KetoneHCID 7909—
ReactantPotassium perfluorobutanesulfonateHCID 23675274—
ReactantHCID 86658629HCID 86658629—
SolventWaterHCID 962—
ProductHCID 87403260HCID 8740326092%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09069245B2
Source datasetuspto-grants-2015_06
ORD IDord-655e5d9a15254debbae47c8a673c26a9
Source noteuspto-grants-2015_06