Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179832Generated: October 30, 2026

Methyl Isobutyl Ketone → HCID 131733079, compound

https://huagongshe.com/reaction/2179832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Isobutyl KetoneHCID 7909—
ReactantLithium bis((trifluoromethyl)sulfonyl)azanideHCID 3816071—
ReactantHCID 86658629HCID 86658629—
SolventWaterHCID 962—
ProductHCID 131733079HCID 13173307987%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09069245B2
Source datasetuspto-grants-2015_06
ORD IDord-152be1b6d37247bc9cfc3619f60a256d
Source noteuspto-grants-2015_06